Zaspopathy
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| Zaspopathy | |
|---|---|
| Other names | Late-onset distal myopathy, Markesbery-Griggs type |
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| Zaspopathy has an autosomal dominant pattern of inheritance. | |
Zaspopathy,[1] also called ZASP-related myofibril myopathy,[2] is a novel autosomal dominant[3] form of progressive muscular dystrophy, first described in 2005.