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Autosomal dominant limb-girdle muscular dystrophy type 1D

Synonym(s) LGMD1D
Prevalence <1 / 1 000 000
Inheritance Autosomal dominant
Age of onset Adult
  • G71.0
MeSH -
MedDRA -


Disease definition

Autosomal dominant limb-girdle muscular dystrophy type 1D (LGMD1D) is a limb girdle muscular dystrophy (LGMD ; see this term) characterized by muscular weakness, primarily affecting the pelvic and shoulder girdles with no bulbar weakness or dysarthria.

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