Rippling muscle disease (Q90418): Difference between revisions

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Property / Canonical URI: https://id.who.int/icd/entity/894802822 / rank
 
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CID11:ID_894802822
Property / CURIE: CID11:ID_894802822 / rank
 
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dki-india-ID_894802822
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 17:23, 15 August 2026

Muscular irritability causes muscle stiffness, slowness of movements after rest, exercise-induced muscle pain, and cramp-like sensations. Taps on the muscles evoke rapid contractions, and passive stretching induce involuntary contractions of muscle fibres that roll over the muscle surface, giving the disease its name. RMD usually has an autosomal dominant mode of inheritance, but sporadic cases have also been described. Genetic studies have identified mostly missense mutations in the caveolin-3 gene (CAV3) on chromosome 1q42 that cause reduced expression of sarcolemmal caveolin in RMD.
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ID_894802822
    English
    Rippling muscle disease
    Muscular irritability causes muscle stiffness, slowness of movements after rest, exercise-induced muscle pain, and cramp-like sensations. Taps on the muscles evoke rapid contractions, and passive stretching induce involuntary contractions of muscle fibres that roll over the muscle surface, giving the disease its name. RMD usually has an autosomal dominant mode of inheritance, but sporadic cases have also been described. Genetic studies have identified mostly missense mutations in the caveolin-3 gene (CAV3) on chromosome 1q42 that cause reduced expression of sarcolemmal caveolin in RMD.

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      CID11:ID_894802822
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      dki-india-ID_894802822
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      Concluído
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      13 August 2026
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