Cause
The term "olivopontocerebellar atrophy" is currently used for two hereditary disorders whose genetic basis remains unknown:
| Number | OMIM | Alt. name | Inheritance |
|---|---|---|---|
| OPCA type 2 | 258300 | Fickler-Winkler type OPCA | autosomal recessive |
| OPCA type 5 | 164700 | OPCA with dementia and extrapyramidal signs | autosomal dominant |
Read more about this topic: Olivopontocerebellar Atrophy
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