autosomal recessive limb-girdle muscular dystrophy type 2H

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.

What is autosomal recessive limb-girdle muscular dystrophy type 2H?

autosomal recessive limb-girdle muscular dystrophy type 2H is a medical condition. A condition is a disease, disorder, or abnormal state that affects the body or mind. This page provides educational information only and is not a diagnosis.

If you think you may have autosomal recessive limb-girdle muscular dystrophy type 2H, speak with a qualified healthcare provider for evaluation and guidance.

Symptoms that may be associated with autosomal recessive limb-girdle muscular dystrophy type 2H

Exercise-induced myalgiaFacial palsyNeck flexor weaknessParesthesiaPelvic girdle muscle weaknessProximal muscle weaknessQuadriceps muscle weaknessShoulder girdle muscle weakness

When to seek medical care

Seek medical advice if you have symptoms that are severe, persistent, or affecting your daily life. Emergency care is needed for symptoms like chest pain, difficulty breathing, confusion, or severe weakness.