Belgian Genetic Tests database
Spinocerebellar ataxia type 17
| Name: |
Spinocerebellar ataxia type 17
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| Description: |
Spinocerebellar ataxia type 17 (SCA17) is a rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term). It is characterized by a variable clinical picture which can include dementia, psychiatric disorders, parkinsonism, dystonia, chorea, spasticity, and epilepsy.
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| ORPHAcode: |
98759
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| Synonyms: |
HDL4
Huntington disease-like 4
SCA17
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| XREF(s): | |
| Analyte(s): | |
| Created: |
13 May 2019 - 01:02
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| Changed: |
22 Jun 2023 - 16:14
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