Catalog

Limb-girdle muscular dystrophy 2H, TRIM32 gene mutation

No MMS code

Link to WHO Definition

Limb-girdle muscular dystrophy 2H, TRIM32 gene mutation – http://id.who.int/icd/entity/2020366790

Limb girdle muscular dystrophy (LGMD) 2H belongs to a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved. LGMD 2H is transmitted as an autosomal recessive form.