Skip to main content

Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis



Glycosylphosphatidylinositol biosynthesis defects (GPIBDs) cause a group of phenotypically overlapping recessive syndromes with intellectual disability, for which pathogenic mutations have been described in 16 genes of the corresponding molecular pathway. An elevated serum activity of alkaline phosphatase (AP), a GPI-linked enzyme, has been used to assign GPIBDs to the phenotypic series of hyperphosphatasia with mental retardation syndrome (HPMRS) and to distinguish them from another subset of GPIBDs, termed multiple congenital anomalies hypotonia seizures syndrome (MCAHS). However, the increasing number of individuals with a GPIBD shows that hyperphosphatasia is a variable feature that is not ideal for a clinical classification.


We studied the discriminatory power of multiple GPI-linked substrates that were assessed by flow cytometry in blood cells and fibroblasts of 39 and 14 individuals with a GPIBD, respectively. On the phenotypic level, we evaluated the frequency of occurrence of clinical symptoms and analyzed the performance of computer-assisted image analysis of the facial gestalt in 91 individuals.


We found that certain malformations such as Morbus Hirschsprung and diaphragmatic defects are more likely to be associated with particular gene defects (PIGV, PGAP3, PIGN). However, especially at the severe end of the clinical spectrum of HPMRS, there is a high phenotypic overlap with MCAHS. Elevation of AP has also been documented in some of the individuals with MCAHS, namely those with PIGA mutations. Although the impairment of GPI-linked substrates is supposed to play the key role in the pathophysiology of GPIBDs, we could not observe gene-specific profiles for flow cytometric markers or a correlation between their cell surface levels and the severity of the phenotype. In contrast, it was facial recognition software that achieved the highest accuracy in predicting the disease-causing gene in a GPIBD.


Due to the overlapping clinical spectrum of both HPMRS and MCAHS in the majority of affected individuals, the elevation of AP and the reduced surface levels of GPI-linked markers in both groups, a common classification as GPIBDs is recommended. The effectiveness of computer-assisted gestalt analysis for the correct gene inference in a GPIBD and probably beyond is remarkable and illustrates how the information contained in human faces is pivotal in the delineation of genetic entities.


Inherited deficiencies of glycosylphosphatidylinositol (GPI) biosynthesis are a heterogeneous group of recessive Mendelian disorders that all share a common feature: the function of GPI-linked proteins is compromised due to a defect in GPI anchor synthesis or modification. Most of the enzymes involved in this molecular pathway are known and the biochemical steps are well described [1]. With respect to the effect of genetic mutations on the anchor and the GPI-linked substrate, several subdivisions of the pathway have been in use: 1) early GPI anchor synthesis, 2) late GPI anchor synthesis, 3) GPI transamidase, and 4) remodeling of fatty acids of the GPI anchor after attachment to proteins (Additional file 1: Figure S1).

The last two groups are defined by their molecular actions and comprise the genes GPAA1, PIGK, PIGU, PIGS, and PIGT for the GPI-transamidase and PGAP1, PGAP2, PGAP3, MPPE1, and TMEM8 for fatty acid remodeling. The differentiation between early and late GPI anchor synthesis considers the molecular consequence of the glycosylphosphatidylinositol biosynthesis defect (GPIBD), which was suggested after an important finding from Murakami et al. [2] regarding the release of alkaline phosphatase (AP), a GPI anchor marker: if anchor synthesis is stuck at an earlier step, the transamidase is not activated and the hydrophobic signal peptide of GPI anchor substrates is not cleaved. As soon as the first mannose residue on the GPI anchor has been added by PIGM, the transamidase tries to attach the substrate to the anchor. However, if subsequent steps are missing, the GPI anchored proteins (GPI-APs) might be less stable and hyperphosphatasia was hypothesized to be a consequence thereof.

The activity of the AP was regarded as such a discriminatory feature that it resulted in the phenotypic series of hyperphosphatasia with mental retardation syndrome (HPMRS) 1 to 6, currently comprising the six genes PGAP2, PGAP3, PIGV, PIGO, PIGW, and PIGY [3,4,5,6,7,8,9]. Whenever a pathogenic mutation was discovered in a new gene of the GPI pathway and the developmentally delayed individuals showed elevated AP in the serum, the gene was simply added to this phenotypic series. If hyperphosphatasia was missing, the gene was linked to another phenotypic series, multiple congenital anomalies hypotonia seizures (MCAHS), that currently consists of PIGA, PIGN, and PIGT [10,11,12]. However, the convention of dividing newly discovered GPIBDs over these two phenotypic subgroups is only reasonable if they really represent distinguishable entities. This practice is now challenged by a growing number of exceptions. The expressivity of most features is variable and even the AP seems to be a biomarker with some variability: some individuals with mutations in PIGA also show elevated AP levels [10, 13,14,15], and some individuals with mutations in PIGO, PIGW, PGAP2, and PGAP3 show AP levels that are only borderline high [16,17,18,19,20].

Recently, deleterious mutations were identified in PIGC, PIGP, and PIGG in individuals with intellectual disability (ID), seizures, and muscular hypotonia, but other features considered to be a prerequisite for MCAHS or HPMRS were missing [21,22,23]. Despite the large phenotypic overlap with most GPIBDs, a flow cytometric analysis of granulocytes in individuals with PIGG mutations did not show reduced surface levels for GPI-APs [21,22,23]. However, Zhao et al. [24] showed that an impairment of PIGG in fibroblasts affects the marker expression, indicating that there might also be variability depending on the tissue. In concordance with these finding, a case report of an individual with ID and seizures that has mutations in PIGQ seems suggestive of a GPIBD in spite of negative FACS results [25].

The work of Makrythanasis et al. [23] can also be considered as a turning point in the naming convention of phenotypes that are caused by deficiencies of the molecular pathway as OMIM has now started referring to them as GPIBDs (see OMIM entry #610293 for a discussion). In this work we go one step further in this direction and ask whether the phenotypic series MCAHS and HPMRS should also be abandoned in favor of a more gene-centered description of the phenotype, which would also be in accordance with what Jaeken [26] already suggested for other congenital disorders of glycosylation. Referring to GPIBD phenotypes in a gene-specific manner makes particular sense if the gene can be predicted from the phenotypic level with some accuracy. For this purpose, we systematically analyzed the discriminatory power for GPIBDs for previously reported individuals as well as 23 novel cases that were identified through routine diagnostics. This also adds novel FACS results for 16 patients (blood or fibroblasts) as well as 19 novel mutations (Additional file 1: Figure S2).

Apart from founder effects that explain the reoccurrence of certain mutations at higher frequency, pathogenic mutations have now been reported in many exons (Additional file 1: Figure S2). However, not much is known about genotype–phenotype correlations in these genes, which makes bioinformatics interpretation of novel variants challenging. The phenotypic analysis, for which we received ethics approval from the Charité University and obtained informed consent from the responsible persons on behalf of all study participants, is based on three different data sources: 1) a comprehensive clinical description of the phenotypic features in human phenotype ontology terminology [27]; 2) flow cytometric profiles of multiple GPI-linked markers; and 3) computer-assisted pattern recognition on frontal photos of individuals with a molecularly confirmed diagnosis.

The rationale behind flow cytometry and image analyses is that GPIBDs might differ in their effect on GPI-APs and their trafficking pathways, resulting in distinguishable phenotypes. Interestingly, we found that the facial gestalt was well suited for delineating the molecular entity. The high information content of facies has become accessible recently through advanced phenotypic tools that might also be used for the analysis of other pathway disorders. Before we present the flow cytometry and automated image analysis results we review the most important phenotypic features of GPIBDs in the old schema of phenotypic series HPMRS and MCAHS.


Clinical overview of HPMRS

HPMRS, which is also sometimes referred to as Mabry syndrome (HPMRS1-6: MIM 239300, MIM 614749, MIM 614207, MIM 615716, MIM 616025, MIM 616809), can present as an apparently non-syndromic form of ID at one end of the clinical spectrum but also as a multiple congenital malformation syndrome at the other end (Table 1). The distinct pattern of facial anomalies of Mabry syndrome consist of wide set eyes, often with a large appearance and upslanting palpebral fissures, a short nose with a broad nasal bridge and tip, and a tented upper lip. The results of a computer-assisted comparison of the gene-specific facial gestalt is given in the “Comparison of the facial gestalt of GPIBDs” section.

Table 1 Summary of clinical findings in patients carrying PIGV, PIGO, PGAP2, PGAP3, PIGW, and PIGY mutations

Psychomotor delay, ID, and variable AP elevation are the only consistent features of all individuals with pathogenic mutations in PIGV [9, 28,29,30,31,32,33,34], PIGO [7, 16, 17, 31, 35,36,37], PGAP2 [4, 8, 18, 38], PGAP3 [5, 19, 39,40,41], and PIGY [6]. Speech development, especially expressive language, is more severely affected than motor skills in the majority of the affected individuals (Table 1). Absent speech development was observed in more than half of the affected individuals. Speech difficulties may be complicated by hearing loss, which is present in a minority of affected individuals. In the different genetic groups, seizures of various types and onset are present in about 65% of affected individuals. Most affected individuals show a good response to anticonvulsive drugs, but a few affected individuals are classified as drug resistant and represent the clinically severe cases (individual 14-0585). Muscular hypotonia is common in all types of HPMRS (about 85%). Behavioral problems, in particular sleep disturbances and autistic features, tend to be frequent (81%) in affected individuals with PGAP3 mutations and are described in a few affected individuals with PIGY mutations but are not documented in affected individuals with mutations in the other four genes. Furthermore, ataxia and unsteady gait have been documented in almost half of the affected individuals carrying PGAP3 mutations and about a third of this group did not achieve free walking at all.

Elevated values of AP were the key finding in affected individuals. However, a few cases are documented with only minimal elevation of this parameter. The degree of persistent hyperphosphatasia in the reported affected individuals varies over a wide range between about 1.1 and 17 times the age-adjusted upper limit of the normal range. The mean elevation of AP is about five to six times the upper limit. Measurements at different ages of one individual show marked variability of this value, for example, from two to seven times the upper limit. There is no association between the AP activity and the degree of neurological involvement. Furthermore, there is no correlation between the mutation class and genes with the level of elevation of AP.

Growth parameters at birth are usually within the normal range. Most affected individuals remain in the normal range, although there is evidence of a skewed distribution towards the upper centiles and a few affected individuals become overweight. In contrast, about 8% of the affected individuals develop postnatal short stature and fail to thrive. About 28% of affected individuals develop microcephaly, whereas less than 10% become macrocephalic. Abnormalities of growth and head size do not correlate with a specific mutation or gene within this group of genes.

Involvement of other organ systems varies among the genetically different groups. PIGV, PIGO, and PGAP2 affected individuals frequently suffer from a variety of different malformations. Anorectal malformations, such as anal atresia or anal stenosis, are the most frequent anomalies with almost 30% penetrance in the group of affected individuals. The second most frequent anomaly is Hirschsprung disease with a frequency of about 26% in the same group of affected individuals. Vesicoureteral or renal malformations occur with a similar frequency; among these are congenital hydronephrosis, megaureter, and vesicoureteral reflux. Our data revealed a frequency of heart defects of about 20% in the group of affected individuals with PIGV, PIGO, and PGAP2 mutations; however, the type of cardiac abnormality is variable. Only 2 of 26 affected individuals carrying PGAP3 mutations have variable congenital heart defects. Cleft palate is the malformation with the highest frequency in the group of affected individuals with PGAP3 mutations with a prevalence of almost 60%, whereas other malformations are rarely observed. Exceptional is a group of ten Egyptian individuals with the same founder mutation and a high incidence of structural brain anomalies (thin corpus callosum (8/10), vermis hypoplasia (4/10), ventriculomegaly (3/10), and Dandy-Walker malformation (1/10)) [39]. To date these are the few individuals with a presumably complete loss of function for this gene (NM_033419.3:c.402dupC, p.Met135Hisfs*28; c.817_820 delGACT, p.Asp273Serfs*37).

Malformations had not been observed in the single reported affected individual with PIGW mutations [3]. Apart from dilation of renal collecting systems, affected individuals with PIGY mutations presented with a new spectrum of organ involvement such as cataracts, rhizomelic shortness of limbs, contractures and hip dysplasia [6].

All affected individuals with PIGV and PIGO mutations had a variable degree of distal hand anomalies, namely brachytelephalangy. They showed hypoplastic finger nails as well as hypoplastic distal phalanges in hand X-rays. Often, they displayed broad and short distal phalanges of the thumbs and halluces, including short and broad corresponding nails of the affected digits. Brachytelephalangy is not present in any of the affected individuals with PGAP3, PGAP2, and PIGW mutations, respectively, although one-third showed broad nails without radiological abnormalities in the available X-rays. One of four affected individuals with PIGY mutations showed brachytelephalangy.

A multidisciplinary approach is required to manage the GPIBDs described in this section, as the clinical variability is broad. It is recommended that all affected individuals have at least one baseline renal ultrasound investigation as well as echocardiography to rule out any obvious malformations. In case of chronic obstipation, Hirschsprung disease, as well as anal anomalies, should be excluded. Hearing evaluation is recommended in all affected individuals. Individuals with behavioral problems may benefit from a review by a clinical psychologist. Regular developmental assessments and EEG investigations are required to ensure that affected individuals get optimal support. The tendency towards epilepsies has been reported to decrease in some affected individuals with age and if the affected individual and physician agree to a trial discontinuation of therapy, medications could be tapered.

Clinical overview of MCAHS

MCAHS comprises a group of genetically different disorders characterized by early onset forms of different types of epilepsies with poor prognosis, missing or minimal psychomotor development, and often, early death (Table 2). The phenotypic series include individuals with PIGA (MIM 300868) [10, 13,14,15, 42,43,44,45,46], PIGN (MIM 614080) [12, 18, 47,48,49,50,51,52,53], and PIGT (MIM 615398) [11, 40, 54,55,56,57] mutations.

Table 2 Comparison of phenotypic data and biomarkers in different types of MCAHS

Neonatal muscular hypotonia is often present. The variable congenital anomalies affect the renal/vesicoureteral, cardiac, and gastrointestinal systems. Brain imaging showed variable abnormalities, for example, thin corpus callosum, cerebellar atrophy/hypoplasia, cerebral atrophy, and delayed myelination, but also normal findings in other affected individuals. There is overlap with the spectrum of malformations seen in HPMRS. Exceptions are megacolon, which is only reported in individuals with PIGV, PIGO, and PGAP2 mutations, and diaphragmatic defects, which are only documented in three fetuses with PIGN mutations [51]. In addition, joint contractures and hyperreflexia are documented in some individuals with PIGA and PIGN mutations [10, 13,14,15, 42,43,44,45,46]. Macrocephaly or macrosomia occur in some of these individuals, whereas microcephaly occurs in others. No distinct facial phenotype is recognizable in comparison within and between the genetically different groups of MCAHS.

Interestingly, 5 out of 23 individuals with PIGA mutations had elevated AP measurements, whereas only one individual with PIGN mutations was reported with borderline high AP activity [52]. In contrast, some of the individuals with PIGT mutations showed decreased AP [11, 54].

HPMRS and MCAHS display an overlapping clinical spectrum but MCAHS has a considerably worse prognosis due to early onset and often intractable seizures as well as early death in the majority of affected individuals. However, facial dysmorphisms do not appear to be characteristic in the different types of MCAHS in contrast to HPMRS. Importantly, elevation of AP and reduced surface levels of GPI-linked substrates are not restricted to HPMRS.

Flow cytometry

Flow cytometry analysis of blood

Flow cytometry was performed on granulocytes extracted from peripheral blood draws that were sampled in BCT CytoChex tubes (Streck, NE, USA), shipped, and analyzed in less than 72 h. Whole blood (50 μl) was mixed with 20 μl of an antibody panel:

  1. 1.

    4 μl CD55-PE (BD #555694), 4 μl CD59-FITC (BD #555763), 2 μl CD45-PacBlue (Beckman Coulter, clone J.33), and 10 μl FACS buffer.

  2. 2.

    2 μl CD16-PE (Beckman Coulter, clone 3G8), 4 μl FLAER-AF488 (FL2S-C; Burlington, Canada,), 2 μl CD45-PacBlue (Beckman Coulter, clone J.33), and 12 μl FACS buffer.

  3. 3.

    2 μl CD24-APC (MiltenyiBiotec Clone REA832), 2 μl CD45-PacBlue (Beckman Coulter, clone J.33), and 16 μl FACS buffer.

The staining was incubated for 30 min at room temperature followed by an incubation with 500 μl red blood cell lysis buffer for 10 min. Debris was removed by discarding the supernatant after centrifugation and the cell pellet was washed twice with 200 μl and resuspended in 100 μl FACS buffer for flow cytometry analysis on a MACSQuant VYB (MiltenyiBiotec, Bergisch Gladbach, Germany).

Gating for living cells was based on forward and side scatter (FSC-A vs. SSC-A). Single cells were gated on a diagonal (FSC-A vs. FSC-H). Granulocytes were identified as granular (SSC-A high) and CD45-positive cells.

The reduction of GPI-AP expression was assessed by the ratio of the median fluorescence intensity (MFI) of the patient to the MFI of a shipped healthy control. Heterozygous carriers of pathogenic mutations (parents) were used as controls when unrelated healthy controls were not available. It is noteworthy that differences in GPI-AP expression were subtle in healthy parents compared to unrelated controls. To compare marker reduction of published and unpublished cases only FLAER and CD16 were used.

Flow cytometric analysis of fibroblast cells

Fibroblasts derived from skin biopsies of patients, parents, and healthy control individuals were cultured in DMEM supplemented with 10% FCS, 1% ultraglutamine, 1% penicillin/streptomycin. For flow cytometry analysis confluently grown cells were washed twice with PBS (-Ca2+, -Mg2+); the cells were gently detached from the coulter dish with Trypsin-EDTA (0.01%). The single cell suspension was washed with FACS buffer, counted, diluted (100.000 cells/stain), and centrifuged, after which the supernatant was discarded and the cell pellet was resuspended in the following antibody mix.

  1. 1.

    4 μl CD55-PE (BD #555694), 4 μl CD59-FITC (BD #555763), and 12 μl FACS buffer.

  2. 2.

    4 μl CD73-PE (BD#550257), 4 μl FLAER-AF488 (Cedarlane, FL2S-C), and 12 μl FACS buffer.

The staining was incubated for 30 min at room temperature followed by two washing steps with 200 μl FACS buffer. For flow cytometry analysis on a MACSQuant VYB the cells were resuspended in 100 μl FACS buffer.

Reduction of GPI-AP expression was calculated as a ratio between the median fluorescence intensity (MFI) of the patient against the mean of MFIs from healthy parents and a healthy unrelated control. It is noteworthy that heterozygous carriers of pathogenic mutations (parents) and unrelated healthy controls had only subtle differences in GPI-AP expression.

Computer-assisted phenotype comparison

Facial images of all individuals with a molecularly confirmed GPIBD were assessed with the Face2Gene Research Application (FDNA Inc., Boston MA, USA). This software tool set allows the phenotypic comparison of user-defined cohorts with ten or more individuals. The classification model of Face2Gene Research uses a neural network architecture that consists of ten convolutional layers, each but the last followed by batch normalization. The original collections are split into training and test sets for cross-validation and mean accuracies for the classification process are computed. The result of a single experiment is a confusion matrix that describes the performance of the classification process. As cohort size is a known confounder, we randomly sampled all cohorts down to the same size (n = 10) and computed the mean true positive and error rates as well as the standard deviation from ten iterations [58]. The scripts for the simulations are available on request and can be used to reproduce the results.


Flow cytometric assessment of GPIBDs

We acquired fibroblast cultures of affected individuals to perform measurements under the same experimental conditions repeatedly. The marker FLAER, which binds to the GPI anchor directly, as well as the GPI-APs CD55, CD59, and CD73, which show high expression levels on fibroblasts, were assessed (Fig. 1). We hypothesized that measuring cell surface levels of GPI-linked substrates directly by flow cytometry might be more suitable to quantify the severity of a GPIBD or to predict the affected gene. No significant differences between patients with MCAHS were observed compared to patients with HPMRS (Fig. 1a). Furthermore, the cell surface levels of CD55 and CD59 were on average lower in cells that were derived from individuals with mutations in PGAP3 compared to individuals with mutations in PIGV (Additional file 1: Table S1), although this did not correspond to a higher prevalence of seizures or a more severe developmental delay. CD55 and CD59 are of particular interest as they protect cells from an attack on the activated complement system and the membrane attack complex that has also been shown to be involved in the pathogenesis of seizures [59].

Fig. 1
figure 1

Flow cytometric profiling for GPIBDs. Cell surface levels of FLAER and tissue-specific GPI-anchored proteins were assessed on fibroblasts (a) as well as on granulocytes (b) of individuals affected by GPIBDs. The relative expression was grouped for GPIBDs of the same phenotypic series, MCAHS (PIGA, PIGN, PIGT) and HPMRS (PGAP3, PIGV, PIGO, PIGW), but showed no significant differences (significance was tested with Wilcoxon-Mann-Whitney test; the p value was corrected for sample size (Bonferoni))

The samples with pathogenic mutations in PIGV are noteworthy as they are derived from individuals that differ considerably in the severity of their phenotype: 14-0585 was born with multiple malformations and his seizures are resistant to treatment, whereas the other three individuals, A2, A3, and P1, are considered to be moderately affected. The flow cytometric profiles, however, do not show marked differences. Furthermore, the cell surface levels of CD55 and CD59 were on average lower in cells that were derived from individuals with mutations in PGAP3.

While the reproducibility of the flow cytometric data on fibroblasts is attractive, the small size of the sample set is clearly a disadvantage in the assessment of potential differences between the phenotypic subgroups of GPIBDs. Most flow cytometric analyses have been performed on granulocytes of affected individuals with the markers CD16 and FLAER and we added a comparison of the relative median fluorescent intensities (rMFI) for a total of 39 individuals of the phenotypic series MCAHS and HPMRS (Additional file 1: Table S2). Although individuals of the MCAHS spectrum are usually more severely affected than individuals of the HPMRS spectrum, we did not observe any significant differences for the tested markers (Fig. 1b). Thus, no significant correlation between FACS profiles of the two phenotypic series was found.

Comparison of the facial gestalt of GPIBDs

The craniofacial characteristics of many Mendelian disorders are highly informative for clinical geneticists and have also been used to delineate gene-specific phenotypes of several GPIBDs [3,4,5, 10, 12, 19, 28,29,30, 32, 39, 40, 43, 44, 60, 61]. However, our medical terminology is often not capable of describing subtle differences in the facial gestalt. Therefore, computer-assisted analysis of the gestalt has recently received much attention in syndromology and several groups have shown that the clinical face phenotype space (CFPS) can also be exploited by machine learning approaches [62]. If a recognizable gestalt exists, a classifier for facial patterns can be trained to infer likely differential diagnoses. Conversely, if photos of affected individuals with disease-causing mutations in different genes of a pathway form separate clusters, it indicates that the gestalt is distinguishable to a certain extent. FDNA’s recently launched RESEARCH application is a deep learning tool for exactly this purpose ( a classification model is generated on two or more collections of frontal images and the performance is reported as a confusion matrix. If true positive rates for the single gene–phenotypes are achieved that are significantly better than for a random assignment of photos to cohorts, there is some phenotypic substructure and the null hypothesis of perfect heterogeneity may be rejected.

We used the RESEARCH app of the Face2Gene suite to evaluate a classifier for the five most prevalent GPIBDs, PIGA (n = 20), PIGN (n = 11), PIGT (n = 12), PIGV (n = 25), and PGAP3 (n = 23). Our original sample set thus consists of frontal facial photos of 91 individuals with a molecularly confirmed diagnosis of HPMRS or MCAHS, including cases that have been previously published [5, 9,10,11, 13,14,15, 19, 28,29,30, 32,33,34, 39, 43, 47, 49, 50, 52,53,54,55,56, 60, 63]. The mean accuracy that was achieved on this original sample set was 52.2%, which is significantly better than random. In order to compare the performance for the single gene classes we had to exclude confounding effects from unbalanced cohort sizes and sampled the cohorts down to the same size of n = 10. Although this decreases the overall performance, the mean accuracy of 45.8% is still significantly better than the 20% that would be achieved by chance in a five-class problem for evenly sized cohorts (Fig. 2). Furthermore, for every single gene–phenotype, the true positive rate (TPR) was better than randomly expected, with PIGV achieving the highest value (59%).

Fig. 2
figure 2

Automated image analysis for five of the most prevalent GPIBDs. A model for the classification of the gene–phenotypes was repeatedly trained and cross-validated on patient subsets that were randomly down-sampled to the same cohort size of n = 10. A mean accuracy of 0.44 was achieved, which is significantly better than random (0.20). For explanatory purposes, the rows of the confusion matrix start with instances of previously published or newly identified individuals with GPIBDs. If the predicted gene matches the molecularly confirmed diagnosis, such a test case would contribute to the true positive rate, shown on the diagonal. Actual affected individual photographs were used to generate an averaged and de-identified composite photo and are shown at the top of the columns. The performance of computer-assisted image classification is significantly better than expected under the null model of perfect heterogeneity and indicates a gene-specific phenotypic substructure for the molecular pathway disease. Higher false positive error rates occur between genes of the same phenotypic series, HPMRS and MCAHS, as indicated by the dendrogram

Interestingly, we observed the highest false negative rate in the confusion matrix for PGAP3 (HPMRS4): on average 32% of these cases are erroneously classified as PIGV (HPMRS1) cases. This finding is in good agreement with the phenotypic delineation from syndromologists that grouped these to genes in the same subclass. A cluster analysis of the confusion matrix actually reproduces the two phenotypic series as shown by the dendrogram in Fig. 2.

While the confusion matrix on the entire sample set can be used to decide whether there are gene-specific substructures in the GPI pathway, pairwise comparisons are better suited to derive phenotypic differences between genes even inside a phenotypic series. We therefore evaluated the area under the receiver operating characteristics curve (AUC) and found the correct gene prediction more often than randomly expected, including PIGV versus PGAP3 (Additional file 1: Figure S3). The differences in pair-wise comparison between PIGV and PGAP3 could be confounded by the large number of Egyptian cases in the PGAP3 cohort [39], the effect of which we could not further analyze due to the limited set of patient photos.


The identification of multiple affected individuals with GPIBDs has enabled the analysis of genotype–phenotype relationships for the molecular pathway of GPI anchor synthesis. Besides a developmental delay and seizures, which are common findings in most affected individuals with a GPIBD, the clinical variability and the variation in expressivity is wide. So far, recognizable gene-specific phenotypes seem to be accepted for PIGL and are discussed for PIGM [64, 65]. For other GPIBDs the phenotypic series HPMRS and MCAHS have been used to subgroup the pathway and the activity of AP in serum was the main classification criterion. However, these disease entities are increasingly cumbersome as some cases are now known to not follow this oversimplified rule.

We therefore compared GPIBDs based on deep phenotyping data and flow cytometric profiles of GPI-APs. Among the 16 genes of the GPI pathway with reports of affected individuals, mutations in PIGA, PIGN, PIGT, PIGV, and PGAP3 were most numerous and these GPIBDs were also suitable for automated image analysis.

A systematic evaluation of the phenotypic features showed that certain malformations occur with a higher frequency in specific GPIBDs. To date, megacolon has only been found to be associated with PIGV, PIGO, and PGAP2 mutations. Diaphragmatic defects have only been documented in affected individuals with PIGN mutations. Only in individuals with PGAP3 mutations are behavioral problems, especially sleep disturbances and autistic features, present, in about 90%. In addition, ataxia and unsteady gait are also frequently documented in this group but not in the others. An accurate classification that is merely based on clinical symptoms is, however, not possible due to their high variability. Also, flow cytometric analysis of GPI marker expression was not indicative for the gene defect and did not correlate with the severity of the phenotype. Of note, however, an assessment of the GPI-AP expression levels seems more sensitive in fibroblasts than in blood cells [24]. This might also be related to the trafficking pathways of GPI-APs through endoplasmic reticulum and Golgi that differ for cell types and substrates [66, 67].

The overlapping clinical spectrum of both HPMRS and MCAHS, the findings of elevated AP, and the reduced surface levels of GPI-linked proteins in some of the MCAHS cases favor a common classification as GPIBDs.

In light of the high variability and expressivity of the clinical findings and the weak genotype–phenotype correlation, the most surprising finding of our study was the high discriminatory power that facial recognition technology achieved. In spite of the similarity of the pathophysiology, differences in the gestalt are still perceptible. This illustrates the remarkable information content of human faces and advocates for the power of computer-assisted syndromology in the definition of disease entities.

Automated image analysis of syndromic disorders is a comparably new field of research and the approach that we used requires photos of at least ten individuals per cohort. However, it is currently not known if there is a minimum number of cases that is required to assess whether a gene–phenotype is recognizable. Furthermore, for every rare disorder with a characteristic gestalt there is possibly a maximum value for the recognizability. So far, the approximation of this upper limit has not systematically been studied depending on the number of individuals that were used in the training process and should definitely be a focus for future research.


A gene-centered classification of GPIBDs is recommended due to the overlapping clinical spectrum of both HPMRS and MCAHS in the majority of affected individuals. Measuring AP serum activity and cell surface levels of GPI-linked markers is still regarded as an imperative in the diagnostic work-up of GPIBDs, especially when dealing with mutations that have not been reported previously. In addition, next-generation phenotyping tools can add another layer of information in the interpretation of novel mutations in the GPI anchor pathway, particularly if the flow cytometric data are inconclusive.



Alkaline phophatase




Area under the curve


Dulbecco's modified Eagle medium


Deep Phenotyping for Deep Learning




Fluorescence-activated cell sorting


Fetal calf serum


Fluorescein isothiocyanate


Fluorescein-labeled proaerolysin


Forward scatter area


Forward scatter area hight




GPI-anchored protein


GPI biosynthesis defect


Hyperphosphatasia with mental retardation syndrome


Intellectual disability


Multiple congenital anomalies hypotonia seizures


Media fluorescent intensity


Occipitofrontal head circumference


Phosphate buffered saline




Side scatter area


true positive rate


  1. Kinoshita T, Fujita M, Maeda Y. Biosynthesis, remodelling and functions of mammalian GPI-anchored proteins: recent progress. J Biochem. 2008;144(3):287–94.

    Article  CAS  PubMed  Google Scholar 

  2. Murakami Y, Kanzawa N, Saito K, Krawitz PM, Mundlos S, Robinson PN, Karadimitris A, Maeda Y, Kinoshita T. Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia-mental retardation syndrome. J Biol Chem. 2012;287(9):6318-6325.

  3. Chiyonobu T, Inoue N, Morimoto M, Kinoshita T, Murakami Y. Glycosylphosphatidylinositol (GPI) anchor deficiency caused by mutations in PIGW is associated with West syndrome and hyperphosphatasia with mental retardation syndrome. J Med Genet. 2014;51(3):203–7.

    Article  CAS  PubMed  Google Scholar 

  4. Hansen L, Tawamie H, Murakami Y, Mang Y, ur Rehman S, Buchert R, Schaffer S, Muhammad S, Bak M, Nothen MM, et al. Hypomorphic mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause autosomal-recessive intellectual disability. Am J Hum Genet. 2013;92(4):575–83.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Howard MF, Murakami Y, Pagnamenta AT, Daumer-Haas C, Fischer B, Hecht J, Keays DA, Knight SJ, Kolsch U, Kruger U, et al. Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation. Am J Hum Genet. 2014;94(2):278-287.

  6. Ilkovski B, Pagnamenta AT, O'Grady GL, Kinoshita T, Howard MF, Lek M, Thomas B, Turner A, Christodoulou J, Sillence D, et al. Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol (GPI) deficiencies. Hum Mol Genet. 2015;24(21):6146-6159.

  7. Krawitz PM, Murakami Y, Hecht J, Kruger U, Holder SE, Mortier GR, Delle Chiaie B, De Baere E, Thompson MD, Roscioli T, et al. Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation. Am J Hum Genet. 2012;91(1):146–51.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Krawitz PM, Murakami Y, Riess A, Hietala M, Kruger U, Zhu N, Kinoshita T, Mundlos S, Hecht J, Robinson PN, et al. PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome. Am J Hum Genet. 2013;92(4):584–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Krawitz PM, Schweiger MR, Rodelsperger C, Marcelis C, Kolsch U, Meisel C, Stephani F, Kinoshita T, Murakami Y, Bauer S, et al. Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nat Genet. 2010;42(10):827–9.

    Article  CAS  PubMed  Google Scholar 

  10. Johnston JJ, Gropman AL, Sapp JC, Teer JK, Martin JM, Liu CF, Yuan X, Ye Z, Cheng L, Brodsky RA, et al. The phenotype of a germline mutation in PIGA: the gene somatically mutated in paroxysmal nocturnal hemoglobinuria. Am J Hum Genet. 2012;90(2):295–300.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Kvarnung M, Nilsson D, Lindstrand A, Korenke GC, Chiang SC, Blennow E, Bergmann M, Stodberg T, Makitie O, Anderlid BM et al. A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT. J Med Genet. 2013;50(8):521-528.

  12. Maydan G, Noyman I, Har-Zahav A, Neriah ZB, Pasmanik-Chor M, Yeheskel A, Albin-Kaplanski A, Maya I, Magal N, Birk E, et al. Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN. J Med Genet. 2011;48(6):383–9.

    Article  CAS  PubMed  Google Scholar 

  13. Fauth C, Steindl K, Toutain A, Farrell S, Witsch-Baumgartner M, Karall D, Joset P, Bohm S, Baumer A, Maier O, et al. A recurrent germline mutation in the PIGA gene causes Simpson-Golabi-Behmel syndrome type 2. Am J Med Genet A. 2016;170A(2):392–402.

    Article  PubMed  Google Scholar 

  14. Kato M, Saitsu H, Murakami Y, Kikuchi K, Watanabe S, Iai M, Miya K, Matsuura R, Takayama R, Ohba C, et al. PIGA mutations cause early-onset epileptic encephalopathies and distinctive features. Neurology. 2014;82(18):1587–96.

    Article  CAS  PubMed  Google Scholar 

  15. van der Crabben SN, Harakalova M, Brilstra EH, van Berkestijn FM, Hofstede FC, van Vught AJ, Cuppen E, Kloosterman W, van Amstel HKP, van Haaften G, et al. Expanding the spectrum of phenotypes associated with germline PIGA mutations: a child with developmental delay, accelerated linear growth, facial dysmorphisms, elevated alkaline phosphatase, and progressive CNS abnormalities. Am J Med Genet A. 2014;164A(1):29–35.

    Article  PubMed  Google Scholar 

  16. Nakamura K, Osaka H, Murakami Y, Anzai R, Nishiyama K, Kodera H, Nakashima M, Tsurusaki Y, Miyake N, Kinoshita T, et al. PIGO mutations in intractable epilepsy and severe developmental delay with mild elevation of alkaline phosphatase levels. Epilepsia. 2014;55(2):e13–17.

    Article  CAS  PubMed  Google Scholar 

  17. Zehavi Y, von Renesse A, Daniel-Spiegel E, Sapir Y, Zalman L, Chervinsky I, Schuelke M, Straussberg R, Spiegel R. A homozygous PIGO mutation associated with severe infantile epileptic encephalopathy and corpus callosum hypoplasia, but normal alkaline phosphatase levels. Metab Brain Dis. 2017;32(6):2131-2137.

  18. Jezela-Stanek A, Ciara E, Piekutowska-Abramczuk D, Trubicka J, Jurkiewicz E, Rokicki D, Mierzewska H, Spychalska J, Uhrynowska M, Szwarc-Bronikowska M, et al. Congenital disorder of glycosylphosphatidylinositol (GPI)-anchor biosynthesis--The phenotype of two patients with novel mutations in the PIGN and PGAP2 genes. Eur J Paediatr Neurol. 2016;20(3):462–73.

    Article  PubMed  Google Scholar 

  19. Knaus A, Awaya T, Helbig I, Afawi Z, Pendziwiat M, Abu-Rachma J, Thompson MD, Cole DE, Skinner S, Annese F, et al. Rare noncoding mutations extend the mutational spectrum in the PGAP3 subtype of hyperphosphatasia with mental retardation syndrome. Hum Mutat. 2016;37(8):737–44.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Hogrebe M, Murakami Y, Wild M, Ahlmann M, Biskup S, Hortnagel K, Gruneberg M, Reunert J, Linden T, Kinoshita T, et al. A novel mutation in PIGW causes glycosylphosphatidylinositol deficiency without hyperphosphatasia. Am J Med Genet A. 2016;170(12):3319–22.

    Article  CAS  PubMed  Google Scholar 

  21. Edvardson S, Murakami Y, Nguyen TT, Shahrour M, St-Denis A, Shaag A, Damseh N, Le Deist F, Bryceson Y, Abu-Libdeh B, et al. Mutations in the phosphatidylinositol glycan C (PIGC) gene are associated with epilepsy and intellectual disability. J Med Genet. 2017;54(3):196–201.

    Article  PubMed  Google Scholar 

  22. Johnstone DL, Nguyen TT, Murakami Y, Kernohan KD, Tetreault M, Goldsmith C, Doja A, Wagner JD, Huang L, Hartley T, et al. Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy. Hum Mol Genet. 2017;26(9):1706–15.

    Article  PubMed  Google Scholar 

  23. Makrythanasis P, Kato M, Zaki MS, Saitsu H, Nakamura K, Santoni FA, Miyatake S, Nakashima M, Issa MY, Guipponi M, et al. Pathogenic variants in PIGG cause intellectual disability with seizures and hypotonia. Am J Hum Genet. 2016;98(4):615–26.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Zhao JJ, Halvardson J, Knaus A, Georgii-Hemming P, Baeck P, Krawitz PM, Thuresson AC, Feuk L. Reduced cell surface levels of GPI-linked markers in a new case with PIGG loss of function. Hum Mutat. 2017;38(10):1394-1401.

  25. Martin HC, Kim GE, Pagnamenta AT, Murakami Y, Carvill GL, Meyer E, Copley RR, Rimmer A, Barcia G, Fleming MR, et al. Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis. Hum Mol Genet. 2014;23(12):3200–11.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Jaeken J. Congenital disorders of glycosylation (CDG): it's (nearly) all in it! J Inherit Metab Dis. 2011;34(4):853–8.

    Article  CAS  PubMed  Google Scholar 

  27. Robinson PN, Kohler S, Bauer S, Seelow D, Horn D, Mundlos S. The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. Am J Hum Genet. 2008;83(5):610–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Horn D, Krawitz P, Mannhardt A, Korenke GC, Meinecke P. Hyperphosphatasia-mental retardation syndrome due to PIGV mutations: expanded clinical spectrum. Am J Med Genet A. 2011;155A(8):1917–22.

    Article  PubMed  Google Scholar 

  29. Thompson MD, Roscioli T, Marcelis C, Nezarati MM, Stolte-Dijkstra I, Sharom FJ, Lu P, Phillips JA, Sweeney E, Robinson PN, et al. Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome). Am J Med Genet A. 2012;158A(3):553–8.

    Article  PubMed  Google Scholar 

  30. Horn D, Wieczorek D, Metcalfe K, Baric I, Palezac L, Cuk M, Petkovic Ramadza D, Kruger U, Demuth S, Heinritz W, et al. Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome. Eur J Hum Genet. 2014;22(6):762–7.

    Article  CAS  PubMed  Google Scholar 

  31. Xue J, Li H, Zhang Y, Yang Z. Clinical and genetic analysis of two Chinese infants with Mabry syndrome. Brain Dev. 2016;38(9):807–18.

    Article  PubMed  Google Scholar 

  32. Reynolds KK, Juusola J, Rice GM, Giampietro PF. Prenatal presentation of Mabry syndrome with congenital diaphragmatic hernia and phenotypic overlap with Fryns syndrome. Am J Med Genet A. 2017;173(10):2776–81.

    Article  CAS  PubMed  Google Scholar 

  33. Rabe P, Haverkamp F, Emons D, Rosskamp R, Zerres K, Passarge E. Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndrome. Am J Med Genet. 1991;41(3):350–4.

    Article  CAS  PubMed  Google Scholar 

  34. Marcelis CL, Rieu P, Beemer F, Brunner HG. Severe mental retardation, epilepsy, anal anomalies, and distal phalangeal hypoplasia in siblings. Clin Dysmorphol. 2007;16(2):73–6.

    Article  PubMed  Google Scholar 

  35. Morren MA, Jaeken J, Visser G, Salles I, Van Geet C, BioResource N, Simeoni I, Turro E, Freson K. PIGO deficiency: palmoplantar keratoderma and novel mutations. Orphanet J Rare Dis. 2017;12(1):101.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Kuki I, Takahashi Y, Okazaki S, Kawawaki H, Ehara E, Inoue N, Kinoshita T, Murakami Y. Vitamin B6-responsive epilepsy due to inherited GPI deficiency. Neurology. 2013;81(16):1467–9.

    Article  PubMed  Google Scholar 

  37. Tanigawa J, Mimatsu H, Mizuno S, Okamoto N, Fukushi D, Tominaga K, Kidokoro H, Muramatsu Y, Nishi E, Nakamura S, et al. Phenotype-genotype correlations of PIGO deficiency with variable phenotypes from infantile lethality to mild learning difficulties. Hum Mutat. 2017;38(7):805–15.

    Article  CAS  PubMed  Google Scholar 

  38. Naseer MI, Rasool M, Jan MM, Chaudhary AG, Pushparaj PN, Abuzenadah AM, Al-Qahtani MH. A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family. J Neurol Sci. 2016;371:121–5.

    Article  CAS  PubMed  Google Scholar 

  39. Abdel-Hamid MS, Issa MY, Otaify GA, Abdel-Ghafar SF, Elbendary HM, Zaki MS. PGAP3-related hyperphosphatasia with mental retardation syndrome: report of 10 new patients and a homozygous founder mutation. Clin Genet. 2017;93(1):84–91.

  40. Pagnamenta AT, Murakami Y, Taylor JM, Anzilotti C, Howard MF, Miller V, Johnson DS, Tadros S, Mansour S, Temple IK, et al. Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders. Eur J Hum Genet. 2017;25(6):669–79.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Nampoothiri S, Hebbar M, Roy AG, Kochumon SP, Bielas S, Shukla A, Girisha KM. Hyperphosphatasia with mental retardation syndrome due to a novel mutation in PGAP3. J Pediatr Genet. 2017;6(3):191–3.

    Article  CAS  PubMed  Google Scholar 

  42. Belet S, Fieremans N, Yuan X, Van Esch H, Verbeeck J, Ye Z, Cheng L, Brodsky BR, Hu H, Kalscheuer VM, et al. Early frameshift mutation in PIGA identified in a large XLID family without neonatal lethality. Hum Mutat. 2014;35(3):350–5.

    Article  CAS  PubMed  Google Scholar 

  43. Swoboda KJ, Margraf RL, Carey JC, Zhou H, Newcomb TM, Coonrod E, Durtschi J, Mallempati K, Kumanovics A, Katz BE, et al. A novel germline PIGA mutation in Ferro-Cerebro-Cutaneous syndrome: a neurodegenerative X-linked epileptic encephalopathy with systemic iron-overload. Am J Med Genet A. 2014;164A(1):17–28.

    Article  PubMed  Google Scholar 

  44. Tarailo-Graovac M, Sinclair G, Stockler-Ipsiroglu S, Van Allen M, Rozmus J, Shyr C, Biancheri R, Oh T, Sayson B, Lafek M, et al. The genotypic and phenotypic spectrum of PIGA deficiency. Orphanet J Rare Dis. 2015;10:23.

    Article  PubMed  PubMed Central  Google Scholar 

  45. Kim YO, Yang JH, Park C, Kim SK, Kim MK, Shin MG, Woo YJ. A novel PIGA mutation in a family with X-linked, early-onset epileptic encephalopathy. Brain Dev. 2016;38(8):750–4.

    Article  PubMed  Google Scholar 

  46. Joshi C, Kolbe DL, Mansilla MA, Mason S, Smith RJ, Campbell CA. Ketogenic diet - A novel treatment for early epileptic encephalopathy due to PIGA deficiency. Brain Dev. 2016;38(9):848–51.

    Article  PubMed  Google Scholar 

  47. Ohba C, Okamoto N, Murakami Y, Suzuki Y, Tsurusaki Y, Nakashima M, Miyake N, Tanaka F, Kinoshita T, Matsumoto N, et al. PIGN mutations cause congenital anomalies, developmental delay, hypotonia, epilepsy, and progressive cerebellar atrophy. Neurogenetics. 2014;15(2):85–92.

    Article  CAS  PubMed  Google Scholar 

  48. Brady PD, Moerman P, De Catte L, Deprest J, Devriendt K, Vermeesch JR. Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic hernia. Eur J Med Genet. 2014;57(9):487–93.

    Article  CAS  PubMed  Google Scholar 

  49. Couser NL, Masood MM, Strande NT, Foreman AK, Crooks K, Weck KE, Lu M, Wilhelmsen KC, Roche M, Evans JP, et al. The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: report and review. Am J Med Genet A. 2015;167A(9):2176–81.

    Article  PubMed  Google Scholar 

  50. Nakagawa T, Taniguchi-Ikeda M, Murakami Y, Nakamura S, Motooka D, Emoto T, Satake W, Nishiyama M, Toyoshima D, Morisada N, et al. A novel PIGN mutation and prenatal diagnosis of inherited glycosylphosphatidylinositol deficiency. Am J Med Genet A. 2016;170A(1):183–8.

    Article  PubMed  Google Scholar 

  51. McInerney-Leo AM, Harris JE, Gattas M, Peach EE, Sinnott S, Dudding-Byth T, Rajagopalan S, Barnett CP, Anderson LK, Wheeler L, et al. Fryns syndrome associated with recessive mutations in PIGN in two separate families. Hum Mutat. 2016;37(7):695–702.

    Article  CAS  PubMed  Google Scholar 

  52. Fleming L, Lemmon M, Beck N, Johnson M, Mu W, Murdock D, Bodurtha J, Hoover-Fong J, Cohn R, Bosemani T, et al. Genotype-phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN-related epilepsy. Am J Med Genet A. 2016;170A(1):77–86.

    Article  PubMed  Google Scholar 

  53. Khayat M, Tilghman JM, Chervinsky I, Zalman L, Chakravarti A, Shalev SA. A PIGN mutation responsible for multiple congenital anomalies-hypotonia-seizures syndrome 1 (MCAHS1) in an Israeli-Arab family. Am J Med Genet A. 2016;170A(1):176–82.

    Article  PubMed  Google Scholar 

  54. Nakashima M, Kashii H, Murakami Y, Kato M, Tsurusaki Y, Miyake N, Kubota M, Kinoshita T, Saitsu H, Matsumoto N. Novel compound heterozygous PIGT mutations caused multiple congenital anomalies-hypotonia-seizures syndrome 3. Neurogenetics. 2014;15(3):193–200.

    Article  PubMed  Google Scholar 

  55. Lam C, Golas GA, Davids M, Huizing M, Kane MS, Krasnewich DM, Malicdan MCV, Adams DR, Markello TC, Zein WM, et al. Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors. Mol Genet Metab. 2015;115(2-3):128–40.

    Article  CAS  PubMed  Google Scholar 

  56. Skauli N, Wallace S, Chiang SC, Baroy T, Holmgren A, Stray-Pedersen A, Bryceson YT, Stromme P, Frengen E, Misceo D. Novel PIGT variant in two brothers: expansion of the multiple congenital anomalies-hypotonia seizures syndrome 3 phenotype. Genes (Basel). 2016;7(12):E108.

  57. Kohashi K, Ishiyama A, Yuasa S, Tanaka T, Miya K, Adachi Y, Sato N, Saitsu H, Ohba C, Matsumoto N et al. Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations. Brain Dev. 2017;40(1):53-57.

  58. Pantel JT, Zhao M, Mensah MA, Hajjir N, Hsieh T-c, Hanani Y, Fleischer N, Kamphans T, Mundlos S, Gurovich Y. Advances in computer-assisted syndrome recognition and differentiation in a set of metabolic disorders.

  59. Xiong ZQ, Qian W, Suzuki K, McNamara JO. Formation of complement membrane attack complex in mammalian cerebral cortex evokes seizures and neurodegeneration. J Neurosci. 2003;23(3):955–60.

    CAS  PubMed  Google Scholar 

  60. Horn D, Schottmann G, Meinecke P. Hyperphosphatasia with mental retardation, brachytelephalangy, and a distinct facial gestalt: Delineation of a recognizable syndrome. European J Med Gen. 2010;53(2):85–8.

    Article  Google Scholar 

  61. Ihara S, Nakayama S, Murakami Y, Suzuki E, Asakawa M, Kinoshita T, Sawa H. PIGN prevents protein aggregation in the endoplasmic reticulum independently of its function in the GPI synthesis. J Cell Sci. 2017;130(3):602–13.

    Article  CAS  PubMed  Google Scholar 

  62. Ferry Q, Steinberg J, Webber C, FitzPatrick DR, Ponting CP, Zisserman A, Nellaker C. Diagnostically relevant facial gestalt information from ordinary photos. Elife. 2014;3:e02020.

    Article  PubMed  PubMed Central  Google Scholar 

  63. Thompson MD, Nezarati MM, Gillessen-Kaesbach G, Meinecke P, Mendoza-Londono R, Mornet E, Brun-Heath I, Squarcioni CP, Legeai-Mallet L, Munnich A, et al. Hyperphosphatasia with seizures, neurologic deficit, and characteristic facial features: Five new patients with Mabry syndrome. Am J Med Genet A. 2010;152A(7):1661–9.

    Article  PubMed  Google Scholar 

  64. Ng BG, Hackmann K, Jones MA, Eroshkin AM, He P, Wiliams R, Bhide S, Cantagrel V, Gleeson JG, Paller AS, et al. Mutations in the Glycosylphosphatidylinositol Gene PIGL Cause CHIME Syndrome. Am J Hum Genet. 2012;90(4):685–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Almeida AM, Murakami Y, Layton DM, Hillmen P, Sellick GS, Maeda Y, Richards S, Patterson S, Kotsianidis I, Mollica L, et al. Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency. Nat Med. 2006;12(7):846–51.

    Article  CAS  PubMed  Google Scholar 

  66. Davis EM, Kim J, Menasche BL, Sheppard J, Liu X, Tan AC, Shen J. Comparative haploid genetic screens reveal divergent pathways in the biogenesis and trafficking of glycophosphatidylinositol-anchored proteins. Cell Rep. 2015;11(11):1727–36.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Muniz M, Riezman H. Trafficking of glycosylphosphatidylinositol anchored proteins from the endoplasmic reticulum to the cell surface. J Lipid Res. 2016;57(3):352–60.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references


The authors thank the patients and their families who participated in this study.


This work was supported by grants from the German Ministry of Research and Education to M.S. (BMBF project number 01EC1402B), and the German Research Foundation to I.H. (HE 5415/6-1), Y.W. (WE 4896/3-1), and P.M.K (KR3985/7-3).

Availability of data and materials

Data supporting the findings of this study are available within the article and Additional file 1. All data that were used for the phenotypic analysis is part of a larger effort, called DPDL, that serves as a case-centered data collection for benchmarking of automated imaging technology. DPDL is accessible at and requires registration. On Face2Gene registered users can run the experiments for phenotypic comparison in the RESEARCH app ( Registration at Face2Gene is free, but is designated to be used by healthcare professionals.

Author information

Authors and Affiliations



AK performed flow cytometry analysis and interpretation. AK, JTP, NH, MZ, TCH, MS, YG, and NF contributed to facial picture acquisition, analysis, and bioinformatics interpretation of the data. MJ and SK performed variant analysis of sequencing data. HM, CK, RSM, AB, PC, NC, HW, SS, RL, CE, MB, HJC, MvdB, EO, AC, ME, FK, NB, HJS, YW, and DH were involved in recruitment of participants, genotyping, and/or phenotypic characterization and interpretation. AK, PNR, SM, DH, IH, and PK were involved in study design and patient data analysis. AK, DH, and PK wrote the manuscript. All authors were involved in interpreting and drafting this manuscript and read and approved the final manuscript.

Corresponding authors

Correspondence to Denise Horn or Peter M. Krawitz.

Ethics declarations

The Charité – Universitätsmedizin Berlin ethics board approved this study, which was carried out in accordance with the principles of the Declaration of Helsinki. Written informed consent to participate was obtained before enrolment from the responsible persons (parents) on behalf of all study participants.

Consent for publication

Written informed consent was obtained before enrolment from the responsible persons (parents) on behalf of all study participants to publish their photographs as well as their clinical data for scientific purposes.

Competing interests

PMK is a member of the scientific advisory board of FDNA, the company providing the Face2Gene platform. YG and NF are employees of FNDA. The remaining authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Additional file

Additional file 1:

Supplemental tables and figures. (DOCX 1270 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Knaus, A., Pantel, J.T., Pendziwiat, M. et al. Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis. Genome Med 10, 3 (2018).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: