Congenital muscular dystrophy 1B

Congenital muscular dystrophy type 1B is a rare, genetic neuromuscular disorder characterized by proximal and symmetrical muscle weakness (particularly of neck, sternomastoid, facial and diaphragm muscles), spinal rigidity, joint contractures (Achilles tendon, elbows, hands), generalized muscle hypertrophy and early respiratory failure (usually in the first decade of life). Patients typically present delayed motor milestones and grossly elevated serum creatine kinase levels, and with disease progression, forced expiratory abdominal squeeze and nocturnal hypoventilation.

Also known as: CMD1B, MDC1B, congenital muscular dystrophy type 1B, muscular dystrophy, congenital, 1B

5 clinical trials for this condition and its sub-types, 0 tagged with Congenital muscular dystrophy 1B itself.