Evidence map›Paper›PMID 42754667›Full record

ArticleEuropean journal of human genetics : EJHG2026

Expanding the genotypic and phenotypic spectrum of PGAP1 deficiency: clinical and functional insights from 15 patients.

Florencia Haase, Oselyne T W Ong, Irene Valenzuela, Adam M Bournazos, Zainab Amasseri, Frenny Sheth, Jayesh Sheth, Harsh Sheth, Rebecca Buchert, Tobias B Haack and 11 more

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In one paragraph

Article in European journal of human genetics : EJHG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Florencia HaaseTranslational Vectorology Research Unit, Children's Medical Research Institute, Westmead, NSW, Australia.ORCID http://orcid.org/0000-0003-4191-9112
Oselyne T W OngTranslational Vectorology Research Unit, Children's Medical Research Institute, Westmead, NSW, Australia.
Irene ValenzuelaClinical and Molecular Genetics Area, Vall d'Hebron Hospital; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.ORCID http://orcid.org/0000-0003-2350-6058
Adam M BournazosThe University of Sydney, Faculty of Medicine and Health, School of Medical Sciences, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0002-6464-4548
Zainab AmasseriMedical Genetics Department, King Faisal Specialist Hospital and Research Centre (KFSHRC), Riyadh, Saudi Arabia.ORCID http://orcid.org/0000-0002-6202-3721
Frenny ShethFoundation for Research in Genetics and Endocrinology (FRIGE), Institute of Human Genetics, Ahmedabad, India.ORCID http://orcid.org/0000-0001-8315-9436
Jayesh ShethFoundation for Research in Genetics and Endocrinology (FRIGE), Institute of Human Genetics, Ahmedabad, India.
Harsh ShethFoundation for Research in Genetics and Endocrinology (FRIGE), Institute of Human Genetics, Ahmedabad, India.ORCID http://orcid.org/0000-0001-9626-0971
Rebecca BuchertInstitute of Medical Genetics and Applied Genomics, Tübingen, Germany.ORCID http://orcid.org/0000-0001-7576-3326
Tobias B HaackInstitute of Medical Genetics and Applied Genomics, Tübingen, Germany.ORCID http://orcid.org/0000-0001-6033-4836
Joris AndrieuxInstitut de Genetique Medicale, Hopital Jeanne de Flandre, CHRU de Lille, Lille, France.
Thomas LiehrInstitute of Human Genetics, Jena University Hospital, Jena, Germany.ORCID http://orcid.org/0000-0003-1672-3054
Alma KuechlerInstitute of Human Genetics Essen, Essen, Germany.
Daniel de Los Reyes HelicesTranslational Vectorology Research Unit, Children's Medical Research Institute, Westmead, NSW, Australia.
Jessica MerjaneTranslational Vectorology Research Unit, Children's Medical Research Institute, Westmead, NSW, Australia.
Sandra T CooperThe University of Sydney, Faculty of Medicine and Health, School of Medical Sciences, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0002-7314-5097
Taroh KinoshitaResearch Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan.ORCID http://orcid.org/0000-0001-7166-7257
Yoshiko MurakamiResearch Institute for Microbial Diseases, The University of Osaka, Suita, Osaka, Japan.
Richard WebsterT.Y. Nelson Department of Neurology and Neurosurgery, Children's Hospital at Westmead, Westmead, NSW, Australia.
Wendy GoldKids Neuroscience Centre, The Children's Hospital at Westmead, Westmead, NSW, Australia.
Leszek LisowskiTranslational Vectorology Research Unit, Children's Medical Research Institute, Westmead, NSW, Australia. llisowski@cmri.org.au.ORCID http://orcid.org/0000-0002-4772-8651

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycosylphosphatidylinositol-anchored proteins (GPI-APs) are essential for neuronal development, synaptic organization and signaling. Defects in GPI-anchor biosynthesis or remodeling cause rare neurodevelopmental disorders, including post-GPI attachment to proteins 1 (PGAP1) deficiency. PGAP1 encodes an inositol deacylase required for GPI-anchor remodeling and appropriate trafficking and membrane localization of GPI-APs. Loss of PGAP1 function disrupts GPI-AP processing, but the clinical spectrum remains incompletely defined because reported cohorts are small. We report 15 individuals with biallelic PGAP1 variants from 11 unrelated families identified through international collaboration. Clinical information was collected using a standardized phenotyping questionnaire and review of available clinical records. The most frequently recorded features were developmental delay or intellectual disability, motor developmental delay, speech impairment, facial dysmorphism, hypotonia and seizures. Independent walking was clearly recorded in a minority of individuals, while feeding, ophthalmological, musculoskeletal and neuroimaging findings were recorded in subsets of the cohort. Clinical investigations were performed as part of routine care and were not uniform across sites. Accordingly, source-dependent assessments including MRI, EEG, EMG/NCS, formal ophthalmology, hearing assessment, systemic imaging, IQ/DQ testing, MRC scoring and anthropometric Z-scores are reported descriptively or using available-data denominators. Spasticity, hypertonia or possible peripheral nerve involvement was recorded in some clinical summaries; however, electrophysiological confirmation was not uniformly available, and confirmed peripheral neuropathy was not analyzed as a cohort-level prevalence outcome. Functional studies in selected patient-derived cells or model systems demonstrated PI-PLC resistance of GPI-APs, supporting impaired GPI-anchor remodeling. These findings expand the genotypic and recorded phenotypic spectrum of PGAP1 deficiency.

Identifiers

PMID42754667

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.