All individuals with variants in gene WDFY3

4 entries on 1 page. Showing entries 1 - 4.
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00305526 Individual 12 PubMed: Vissers 2020 2-generation family, 1 affected F - - - - - - - NDD birth 39+4 w, weight 2400 (<-2.5 SD), OFC 37 (normal); height Normal, weight Normal, OFC (+3.0 SD); mild/moderate intellectual disability; developmental delay; motor delay; speech delay; no dysarthria; no epilepsy; hypotonia; no spasticity; no ataxia; attention deficit disorder; no sleep disturbances; facial abnormalities; no cardiac abnormalities; Tendency to chew long time before swallowing; Late ossification of anterior fontanel; Hyperkinesia; MRI-brain no holoprosencephaly, Abnormal corpus callosum with hypertrophic anterior part and thin posterior part, Virchow Robin 1 1 Johan den Dunnen
00415085 202299 - - M - Germany - - - - - MCPH18 neurodevelopmental delay, autistic behavior 1 1 Andreas Laner
00458111 FamPatII1 PubMed: Graziani 2024 2-generation family, affected father/daughter F no Italy white - - yes none macrocephaly/autism syndrome macrocephaly, global developmental delay, autism, lateral ventricle dilatation 1 2 Ludovico Graziani
00458137 family PubMed: Kadir 2016 3-generation family, 10 affected (5F, 5M) F;M no Israel - - - - - MCPH see paper; ..., primary microcephaly, OFC SD<3; mild-moderate intellectual disability; no dysmorphic features, no ocular malformations, no failure to thrive 1 10 Johan den Dunnen
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