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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Muscular Dystrophies > Muscular Dystrophies, Limb-Girdle
... > Nervous System Diseases > Neuromuscular Diseases > Muscular Diseases > Muscular Disorders, Atrophic > Muscular Dystrophies > Muscular Dystrophies, Limb-Girdle
Musculoskeletal Diseases > Muscular Diseases > Muscular Disorders, Atrophic > Muscular Dystrophies > Muscular Dystrophies, Limb-Girdle

Preferred term

Muscular Dystrophies, Limb-Girdle  

Type

  • Topical Descriptor

Broader concept

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Entry terms

  • Limb Girdle Muscular Dystrophies
  • Limb-Girdle Muscular Dystrophies
  • Limb Girdle Muscular Dystrophy
  • Limb-Girdle Muscular Dystrophy
  • Limb-Girdle Syndrome
  • Muscular Dystrophy, Limb Girdle
  • Muscular Dystrophy, Limb-Girdle
  • Myopathic Limb-Girdle Syndrome

Scope note

  • A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).

History note

  • 2005; use MUSCULAR DYSTROPHIES 2000-2004

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URI

http://www.yso.fi/onto/mesh/D049288

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