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Condition

Muscular Dystrophy

Congenital Malformations and Chromosomal Abnormalities

Muscular dystrophy is a group of genetically and clinically varied neuromuscular diseases that cause progressive weakness and deterioration of skeletal muscle over time. The more than thirty recognized types differ in which muscles are affected first, how quickly the disease worsens, and when symptoms begin, and some types are also associated with problems in other organs, including the heart. The disorders are caused by mutations in genes needed to build and maintain healthy muscle tissue.

Facts
Classification
Body System
Muscular System 1
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2
Communicable or Non-communicable
Non-Communicable 3
Transmission Route
Non-Transmissible 3
Connections

Treated By

Physical therapy is standard supportive treatment to maintain mobility and function in muscular dystrophy.

Sources
1. Wikipedia
Wikipedia contributors, Wikimedia Foundationhttps://en.wikipedia.org/wiki/Muscular_dystrophy, lead section
Quote, https://en.wikipedia.org/wiki/Muscular_dystrophy, lead section
Muscular dystrophy (MD) is a genetically and clinically heterogeneous group of rare neuromuscular diseases that cause progressive weakness and breakdown of skeletal muscles over time. The disorders differ as to which muscles are primarily affected, the degree
View the Source
2. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XVII
Quote, List of chapters, Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
View the Source
3. Wikipedia: Non-communicable disease
Wikipedia
  • Lead section, transmission-route statement (inferred from disease-category)
    Down syndrome and Cystic fibrosis.
  • Inherited/genetic diseases section
    Down syndrome and Cystic fibrosis.
View the Source
Wikidata: Muscular Dystrophy
Wikidata Q1137767, class allow-list match (w-wdresolver-0926)View the Source
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