Autosomal recessive limb-girdle muscular dystrophy type 2H (LGMD2H) is a mild subtype of autosomal recessive limb girdle muscular dystrophy characterized by slowly progressive proximal muscle weakness and wasting of the pelvic and shoulder girdles with onset that usually occurs during the second or third decade of life. Clinical presentation is variable and can include calf psuedohypertrophy, joint contractures, scapular winging, muscle cramping and/or facial and respiratory muscle involvement. The disease is autosomal recessive limb-girdle muscular dystrophy type 2H (MONDO_0009683). Also known as: LGMD2H, Sarcotubular myopathy, TRIM32 autosomal recessive limb-girdle muscular dystrophy, autosomal recessive limb-girdle muscular dystrophy caused by mutation in TRIM32, limb-girdle muscular dystrophy due to TRIM32 deficiency, muscular dystrophy Hutterite type, muscular dystrophy, limb-girdle, autosomal recessive 8, sarcotubular myopathy.