All individuals with variants in gene CWF19L1

7 entries on 1 page. Showing entries 1 - 7.
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00037591 - PubMed: Nguyen 2015, Journal: Nguyen 2015 one affected in family, no sibs, parents unaffected heterozygous carriers F no Netherlands white - - - - SCAR17 - 2 1 Mike Gerards
00037743 - PubMed: Yapici 2005; Journal: Yapici 2005 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents and brother M yes Turkey - - - - - SCAR17 see paper; hypotonia, developmental delay, mental retardation, non- progressive truncal and extremity ataxia; MRI demonstrated hypoplasia vermis and cerebellar hemispheres; ... 1 2 Johan den Dunnen
00275648 FamMR106Pat1 PubMed: Santos-Cortez 2018 4-generation family, 3 affected (F, 2M), unaffected heterozygous carrier parents/relatives M yes Pakistan - - - - - ID OFC 46cm; IQ 40, moderate intellectual disability (HP:0002342); developmental delay 1 3 Johan den Dunnen
00275649 FamMR106Pat4 PubMed: Santos-Cortez 2018 - M yes Pakistan - - - - - ID OFC 50cm; IQ 42, moderate intellectual disability (HP:0002342); developmental delay, seizures, ataxia, MRI-brain cerebellar atrophy 1 1 Johan den Dunnen
00362028 PME54 PubMed: Courage 2021, Journal: Courage 2021 - - - - - - - - - epilepsy - 1 1 Johan den Dunnen
00412787 199437 - - M yes Nepal - - - - - SCAR17 Global developmental delay, Cerebellar hypoplasia, Dandy-Walker malformation, Hypoplasia of the corpus callosum, Aplasia/Hypoplasia involving the central nervous system, Intellectual disability, Poor fine motor coordination, Delayed gross motor development, Facial grimacing, Bradyphrenia, Behavioral abnormality, Attention deficit hyperactivity disorder 1 1 Andreas Laner
00415262 17 PubMed: Alfares 2018 - M - - - - - - - retinal disease OMIM: 616127; developmental delay cerebellar atrophy 1 1 LOVD
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