Disease #04243 (SCAR17 (ataxia, spinocerebellar, autosomal recessive, type 17 (SCAR-17)), OMIM:616127)

Official abbreviation SCAR17
Name ataxia, spinocerebellar, autosomal recessive, type 17 (SCAR-17)
OMIM ID 616127
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene CWF19L1
Associated tissues -
Disease features -
Remarks -
Date created 2015-05-01 15:29:36 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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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 - CWF19L1 CWF19L1 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; ... CWF19L1 CWF19L1 1 2 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 CWF19L1 CWF19L1 1 1 Andreas Laner
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