Spinocerebellar ataxia type 9 (SCA9)
Written and reviewed by Dr Ibrahim Imam, Consultant Neurologist. Last reviewed .
Spinocerebellar ataxia type 9 (SCA9). The genetics of SCA9 are unknown. Onset is in adulthood. Fully referenced neurology checklist.
Genetics
- The genetics of SCA9 are unknown
- Onset is in adulthood
Clinical features
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Magnetic resonance imaging (MRI) brain: features
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References
Related checklists
- Spinocerebellar ataxia (SCA) summary of key features
- Spinocerebellar ataxia type 1 (SCA 1)
- Spinocerebellar ataxia type 2 (SCA2)
- Spinocerebellar ataxia type 3 (SCA3): clinical features
- Spinocerebellar ataxia type 3 (SCA3): management
- Spinocerebellar ataxia type 4 (SCA4)
- Spinocerebellar ataxia type 5 (SCA5)
- Spinocerebellar ataxia type 6 (SCA6)
- Spinocerebellar ataxia type 7 (SCA7)
- Spinocerebellar ataxia type 8 (SCA8)
- Spinocerebellar ataxia type 10 (SCA10)
- Spinocerebellar ataxia type 11 (SCA11)
- Spinocerebellar ataxia type 12 (SCA12)
- Spinocerebellar ataxia type 13 (SCA13)
- Spinocerebellar ataxia type 14 (SCA14)
- Spinocerebellar ataxia type 15 (SCA15)
- Spinocerebellar ataxia type 16 (SCA16)
- Spinocerebellar ataxia type 17 (SCA17)
- Spinocerebellar ataxia type 18 (SCA18)
- Spinocerebellar ataxia type 19 (SCA19)
- Spinocerebellar ataxia type 20 (SCA20)
- Spinocerebellar ataxia type 21 (SCA21)
- Spinocerebellar ataxia type 22 (SCA22)
- Spinocerebellar ataxia type 23 (SCA23)
- Spinocerebellar ataxia type 24 (SCA24)
