Autosomal recessive spinocerebellar ataxia with raised alpha-fetoprotein
Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .
Autosomal recessive spinocerebellar ataxia with raised alpha-fetoprotein. This is caused by mutations in chromosome 9q. The onset is in late childhood.
Genetics
- This is caused by mutations in chromosome 9q
- The onset is in late childhood
Clinical features
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Investigations
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References
Related checklists
- Ataxia telangiectasia (AT)
- Ataxia-telangiectasia like disorder (ATLD)
- COQ8A ataxia
- Cayman ataxia
- Cockayne syndrome
- Abetalipoproteinaemia
- Gordon Holmes syndrome (GHS)
- Autosomal recessive spinocerebellar ataxias (SCAR)
- Autosomal recessive cerebellar ataxia with STUB1 mutations
- Spinocerebellar ataxia with axonal neuropathy (SCAN1)
- Infantile-onset spinocerebellar ataxia (IOSCA)
