Welander distal myopathy (Q85554): Difference between revisions
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13 August 2026
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Latest revision as of 10:54, 15 August 2026
Welander distal myopathy is a distal, slowly progressive myopathy with late onset (after the age of 40) inherited as an autosomal dominant trait, presenting with clumsiness in performing fine motor skills with the index finger and thumb followed by progression to all the finger extensor muscles and atrophy of intrinsic hand muscles. Lower limb involvement occurs later.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1107278535 |
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| English | Welander distal myopathy |
Welander distal myopathy is a distal, slowly progressive myopathy with late onset (after the age of 40) inherited as an autosomal dominant trait, presenting with clumsiness in performing fine motor skills with the index finger and thumb followed by progression to all the finger extensor muscles and atrophy of intrinsic hand muscles. Lower limb involvement occurs later. |
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CID11:ID_1107278535
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dki-india-ID_1107278535
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Concluído
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13 August 2026
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