Rippling muscle disease (Q90418): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (4 intermediate revisions by the same user not shown) | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_894802822 | |||||||||||||||
| Property / CURIE: CID11:ID_894802822 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_894802822 | |||||||||||||||
| Property / Canary Token: dki-india-ID_894802822 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 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. |
Statements
CID11:ID_894802822
0 references
dki-india-ID_894802822
0 references
Concluído
0 references
13 August 2026
0 references
