Autosomal dominant benign distal spinal muscular atrophy (Q103452): Difference between revisions
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16 August 2026
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Latest revision as of 09:13, 17 August 2026
Patients with autosomal dominant benign distal spinal muscular atrophy present with lower motor neuron weakness of the lower limb. Weakness is congenital, and arthrogryposis may be observed, suggesting intrauterine onset. Severity of weakness varies within families. Weakness is typically non-progressive. The disease is caused by mutations in the TRPV4 gene (12q24.11).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_741190474 |
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| English | Autosomal dominant benign distal spinal muscular atrophy |
Patients with autosomal dominant benign distal spinal muscular atrophy present with lower motor neuron weakness of the lower limb. Weakness is congenital, and arthrogryposis may be observed, suggesting intrauterine onset. Severity of weakness varies within families. Weakness is typically non-progressive. The disease is caused by mutations in the TRPV4 gene (12q24.11). |
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CID11:ID_741190474
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dki-india-ID_741190474
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Concluído
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16 August 2026
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