All individuals with variants in gene C3orf17

4 entries on 1 page. Showing entries 1 - 4.
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00301741 15DG2238;15DG0764, 15DG0765 PubMed: Maddirevula 2019, PubMed: Maddirevula 2018 family, 2 affected (F, M) F;M yes - Arab - - - - skeletal dysplasia Neonatal hypotonia, Cutis laxa, Global developmental delay, Kyphosis, Joint laxity 1 2 Johan den Dunnen
00331519 15DG2238 , 15DG2239 PubMed: Maddirevula 2018 family, 2 affected (2M) M yes - Arab - - - - skeletal dysplasia Feeding difficulties, Inguinal hernia, Neonatal hypotonia, Recurrent aspiration pneumonia, No 1 2 LOVD
00395614 RP-3055 PubMed: Perea-Romero 2021 - - - Spain - - - - - retinal disease cataract, glaucoma, rod-cone dystrophy, severe myopia, conductive hearing impairment, intellectual disability, renal atrophy, renal insufficiency 1 1 LOVD
00469799 patient;? PubMed: Narayanan 2019, PubMed: Jacob 2025 5-generation family, 1 affected, unaffected heterozygous carrier parents F - India - - - - - skeletal dysplasia see paper; ..., short stature, bilateral genu valga; high anterior hairline, sparse scalp hair, broad medially sparse eyebrows, retrognathia; hands/feet short, mild hypoplastic nails; elbows cubitus valgus with limited extension 1 1 Johan den Dunnen
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