Disease #01564 (SCA6 (ataxia, spinocerebellar, type 6), OMIM:183086)

Official abbreviation SCA6
Name ataxia, spinocerebellar, type 6
OMIM ID 183086
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 3
Associated with 1 gene CACNA1A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-03-22 16:53:30 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00106553 606181126 - Mother is also affected F ? (Germany) - - - no - SCA1, SCA10, SCA11, SCA14, SCA17, SCA27A, SCA5, SCA6, SCA7, SCA8 - FGF14, PRKACG, PRKCG, SPTBN2, TTBK2 PRKCG 1 1 Friederike Hein
00326660 174205 - - M ? Germany - - - - - SCA6 (+) Astigmatism,(+) Ataxia,(+) Short stature,(+) Downbeat nystagmus CACNA1A CACNA1A 1 1 Andreas Laner
00334917 PME16 PubMed: Courage 2021, Journal: Courage 2021 - F no Italy - - - - - SCA6 Progressive ataxia from 30 years of age (possible childhood onset) associated with myoclonus, on a background of mild intellectual impairment and sensorineural hearing impairment. MRI showing cerebellar atrophy and EEG findings of diffuse paroxysmal abnormalities consistent with encephalopathy. No migraine. Family history of epilepsy and possible ataxia affecting father and brother (now deceased). - CACNA1A 1 1 Carolina Courage
00359604 176905 - - M - Germany - - - - - SCA6 clinical suspicion of SCA; (+) Abnormality of the philtrum,(+) Broad philtrum,(+) Muscle weakness,(+) Aplasia/Hypoplasia of fingers,(+) Abnormal ear morphology CACNA1A CACNA1A 1 1 Andreas Laner
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