All individuals with variants in gene KCTD3

6 entries on 1 page. Showing entries 1 - 6.
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00080824 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - ID Severe psychomotor retardation, seizures and cerebellar hypoplasia (PMID:25558065) 1 1 Daniel Trujillano
00225699 25558065-Fam13DG2274 PubMed: Alazami 2015, Journal: Alazami 2015 4-generation family, 4 affected (F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Saudi Arabia - - - - - ? see paper; …, severe psychomotor retardation, seizure, and cerebellar hypoplasia 1 4 Johan den Dunnen
00361614 13DG2274 PubMed: Anazi 2017 familial M no Saudi Arabia - - - - - ID not syndromic; global developmental delay and seizures 1 1 Johan den Dunnen
00387391 11 PubMed: Sun 2020 - F - China - - - - - retinal disease posterior subcapsular cataract, peripheral choroidal atrophy, negative family history, BCVA OD/OS: FC/HM, hearing loss 1 1 LOVD
00387397 17 PubMed: Sun 2020 - F - China - - - - - retinal disease no lens opacity, peripheral choroidal atrophy, negative family history, BCVA OD/OS: 0.15/0.5 1 1 LOVD
00387401 21 PubMed: Sun 2020 - M - China - - - - - retinal disease no lens opacity, peripheral choroidal atrophy, negative family history, BCVA OD/OS: 0.05/0.05, red–green color blindne 1 1 LOVD
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