Limb-girdle muscular dystrophy 1D, gene mapped to 6q23 (Q84668)

Limb girdle muscular dystrophy, type1E (LGMD1E) belongs to a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by onset in late adulthood, possible dysphagia and no evident cardiac abnormalities.