Laing distal myopathy (Q85561): Difference between revisions
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Miopatia distal de Laing, também chamada de miopatia distal, tipo 1 (MPD1), é uma doença muscular autossômica dominante caracterizada por fraqueza seletiva de início precoce dos dorsiflexores do dedão do pé e tornozelo e um curso progressivo muito lentamente. | |||
| description / en | description / en | ||
Laing distal myopathy, also called myopathy distal, type 1 (MPD1), is an autosomal dominant muscle disease characterised by early-onset selective weakness of the great toe and ankle dorsiflexors, and a very slowly progressive course. | |||
Revision as of 10:55, 15 August 2026
Laing distal myopathy, also called myopathy distal, type 1 (MPD1), is an autosomal dominant muscle disease characterised by early-onset selective weakness of the great toe and ankle dorsiflexors, and a very slowly progressive course.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1155662121 |
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| English | Laing distal myopathy |
Laing distal myopathy, also called myopathy distal, type 1 (MPD1), is an autosomal dominant muscle disease characterised by early-onset selective weakness of the great toe and ankle dorsiflexors, and a very slowly progressive course. |
