Autosomal recessive spinocerebellar ataxia with raised alpha-fetoprotein
Evidence-based neurology checklist on autosomal recessive spinocerebellar ataxia with raised alpha-fetoprotein: Genetics This is caused by mutations in chromosome 9q The onset is in late childhood Clinical features Investigations
Genetics
- This is caused by mutations in chromosome 9q
- The onset is in late childhood
Clinical features
Investigations
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)
