Disease #03926 (MCAHS3;GPIBD7 (multiple congenital anomalies, hypotonia, seizures syndrome, type 3 (MCAHS-3, glycosylphosphatidylinositol deficiency, type 7 (GPIBD-7))), OMIM:615398)

Official abbreviation MCAHS3;GPIBD7
Name multiple congenital anomalies, hypotonia, seizures syndrome, type 3 (MCAHS-3, glycosylphosphatidylinositol deficiency, type 7 (GPIBD-7))
OMIM ID 615398
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PIGT
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00207529 Patient 3 PubMed: Kvarnung et al., 2018 - - - - - - - - - MCAHS3;GPIBD7 ID, seizures PIGT PIGT 1 1 Philippe Campeau
00207530 Proband PubMed: Yang et al., 2018 Homozygous PIGT variant in a Chinese boy with multiple malformations, hypotonia, seizure and profound development delay M no China Chinese >00y10m - - Anti-epileptic medications MCAHS3;GPIBD7 Multiple malformations, hypotonia, seizure and profound development delay. Dysmorphic features (high forehead, frontal bossing, narrow bitemporal, big eyes with slight orbital depression, esotropia, depressed nasal bridge, long philtrum, high palatine arch, wide and opening mouth, low auricular position). Hypotonia. Lower limb hyperreflexia. Normal ALP level. MRI shows external hydrocephalus, cortical hypoplasia, cerebellar vermis dysplasia. PIGT PIGT 2 1 Philippe Campeau
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