Distal hereditary motor neuropathy type 1 (Q103443): Difference between revisions
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Revision as of 09:12, 17 August 2026
Patients with DHMN1 develop distal lower limb weakness with or without pes cavus, typically in the first decade of life. Some patients may show increased lower limb muscle tone or extensor plantar responses. Weakness is slowly progressive but life expectancy is normal. Linkage analyses have identified a disease locus at 7q34-q36.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1049436513 |
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| English | Distal hereditary motor neuropathy type 1 |
Patients with DHMN1 develop distal lower limb weakness with or without pes cavus, typically in the first decade of life. Some patients may show increased lower limb muscle tone or extensor plantar responses. Weakness is slowly progressive but life expectancy is normal. Linkage analyses have identified a disease locus at 7q34-q36. |
Statements
CID11:ID_1049436513
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