Welander distal myopathy (Q85554): Difference between revisions
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A miopatia distal de Welander é uma miopatia distal lentamente progressiva com início tardio (após os 40 anos) herdada como um traço autossômico dominante, apresentando-se com dificuldade em realizar habilidades motoras finas com o dedo indicador e o polegar, seguido por progressão para todos os músculos extensores do dedo e atrofia dos músculos intrínsecos da mão. O envolvimento dos membros inferiores ocorre mais tarde. | |||
| description / en | description / en | ||
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. | |||
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. |
