All individuals with variants in gene KLHDC4

5 entries on 1 page. Showing entries 1 - 5.
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00050549 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? hypertelorism, depressed nasal bridge, generalized hypotonia 1 1 Johan den Dunnen
00265339 Fam6PatIV1 PubMed: Dias 2019 - M yes Egypt - - - - - ID intellectual disability/global developmental delay; motor delay; language delay; autistic features/stereotypy; hyperactivity; screaming/laughing spells; no self-injury/hand-biting; bruxism; no hypotonia in infancy; ambulatory; MRI brain abnormalities; seizures; no microcephaly; dysmorphic features; no ophthalmologic features; no gastrointestinal symptoms 1 2 Caroline Dias
00394128 FamPatII2 PubMed: Al-Deri 2021 2-generation family, 3 affected sibs, unaffected heterozygous carrier parents/relatives F no United States Jewish-Ashkenazi - - - - ? unremarkable prenatal/perinatal development; 12m-developmental delay; no illness provoked regression; 12m-sit independently, never crawled, 2y-walk; severe expressive language delay; no tetraplegia; no dystonia, no seizures 1 3 Johan den Dunnen
00394129 FamPatII3 PubMed: Al-Deri 2021 sister F no United States Jewish-Ashkenazi - - - - ? unremarkable prenatal/perinatal development; 4m-developmental delay; no illness provoked regression; very mild motor delay, 15m-walk; severe expressive language delay; no tetraplegia; no dystonia, no seizures 1 1 Johan den Dunnen
00394130 FamPatII4 PubMed: Al-Deri 2021 brother M no United States Jewish-Ashkenazi - - - - ? unremarkable prenatal/perinatal development; MRI brain 2y-normal; 6m-developmental delay; no illness provoked regression; 12m-sit, 18m-crawl, 2-3y-walk; severe expressive language delay; no tetraplegia; no dystonia, no seizures 1 1 Johan den Dunnen
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