Cerebellar ataxia
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| ICD-10 | G111-G113 | |
|---|---|---|
| ICD-9 | 334.3 | |
| OMIM | [1] | |
| DiseasesDB | 2218 | |
| MedlinePlus | 001397 | |
| eMedicine | / | |
| MeSH | {{{MeshNumber}}} | |
Cerebellar ataxia is a form of ataxia originating in the cerebellum.[1]
A rare disease of the rhombencephalon, "rhombencephalosynapsis" is characterized by a missing vermis resulting in a fused cerebellum. Patients generally present with cerebellar ataxia.
Assessment
Edit
Romberg's test can be used to distinguish cerebellar ataxia from other forms of ataxia.
See alsoEdit
ReferencesEdit
- ↑ BBC NEWS. URL accessed on 2007-07-29.
Symptoms and signs: nervous and musculoskeletal systems (R25–R29, 781.0, 781.2–9) | |||||||||||||||||||||
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| Primarily joint | |||||||||||||||||||||
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Lesions of spinal cord and brain | |||||||||||
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| Spinal cord/ vascular myelopathy |
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| Brainstem |
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| Cerebellum |
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| Basal ganglia | |||||||||||
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