A form of muscular dystrophy that usually begins in middle age or later, causing weakness in the muscles of the feet and hands.
| Medical Glossary: Distal muscular dystrophy |
A form of muscular dystrophy that usually begins in middle age or later, causing weakness in the muscles of the feet and hands.
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| Wikipedia: Distal muscular dystrophy |
| Distal muscular dystrophy | |
| Classification and external resources | |
| ICD-10 | G71.0 |
|---|---|
| ICD-9 | 359.1 |
| OMIM | 254130 604454 606768 |
| DiseasesDB | 31977 33507 |
| eMedicine | / |
| MeSH | [1] |
Distal muscular dystrophy (or distal myopathy) is a group of disorders characterized by onset in the hands or feet.
Many types involve dysferlin, but it has been suggested that not all cases do.[1]
Types include:
| Name | OMIM | Locus |
|---|---|---|
| Miyoshi myopathy (in Japan)[2] | 254130 | DYSF at 2p13.3-p13.1 |
| Distal myopathy with anterior tibial onset | 606768 | DYSF at 2p13.3-p13.1 |
| Welander distal myopathy | 604454 | ? at 2p13[3] |
DYSF is also associated with Limb-Girdle muscular dystrophy type 2B.[4]
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This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)
| Muscular Dystrophy | |
| Dysferlin | |
| ICD-10 Chapter VI: Diseases of the nervous system |
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