All individuals with variants in gene PTRH2

5 entries on 1 page. Showing entries 1 - 5.
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00225703 25558065-Fam13DG0215 PubMed: Alazami 2015, Journal: Alazami 2015 6-generation family, 2 affected brothers, unaffected heterozygous carrier parents/relatives M yes Saudi Arabia - - - - - ? see paper; …, global developmental delay, hearing loss, and ataxia 1 2 Johan den Dunnen
00361568 12DG1210 PubMed: Anazi 2017 familial M - Saudi Arabia - - - - - ID not syndromic; global developmental delay 1 1 Johan den Dunnen
00448517 287210 - - F yes Syria Kurdish - - - - IMNEPD Secondary microcephaly, Progressive gait ataxia, Abnormal foot morphology, Intellectual disability, Sensorineural hearing impairment, Neurodevelopmental delay 1 1 Andreas Laner
00472798 Pat2 PubMed: Murdock 2021 2-generation family, 1 affected M - United States - - - - - ? see paper; ..., intellectual disability (IQ60-70), dysmorphism; global developmental delay, 2y6m-walk, <5y-first words; maladaptive behavior (aggressive, self-harm, violent outbursts, refusal to eat), G-tube placement; chronic constipation, seizures; hypertelorism, broad forehead, low posterior hairline, hypotonia 1 1 Johan den Dunnen
00473984 Fam9915157Pat1519 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history F yes Iran - - - - - ataxia Asphyxia at birth; Developmental delay, mental & motor; Mental retardation; Speech problem; Delayed walking; Cerebellar ataxia, since 2y, Neurodegenerative disorders; Hypothyroidism; Anemia; Hyperactivity; Behavioral problems; Atrophy of the cerebellum in brain MRI 1 1 Johan den Dunnen
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