Autosomal dominant limb-girdle muscular dystrophy type 1C (LGMD1C) is a limb girdle muscular dystrophy (LGMD; see this term) caveolinopathy characterized by weakness in limb-girdle muscles, calf muscle hypertrophy and lack of respiratory and cardiac involvement. The disease is Orphanet_265 (Autosomal dominant limb-girdle muscular dystrophy type 1C). Also known as: LGMD1C, Limb-girdle muscular dystrophy due to caveolin-3 deficiency.