/congenital merosin-deficient muscular dystrophy 1A

congenital merosin-deficient muscular dystrophy 1A

Rare Disease

MONDO:0011925

Also Known As

CMD1ALAMA2 congenital muscular dystrophyMDC1Acongenital merosin-deficient muscular dystrophy type 1Acongenital muscular dystrophy caused by mutation in LAMA2congenital muscular dystrophy due to laminin alpha2 deficiencymerosin-deficient congenital muscular dystrophy type 1Amerosin-negative congenital muscular dystrophymuscular dystrophy, congenital merosin-deficient, type 1Amuscular dystrophy, congenital, merosin deficient or partially deficientLAMA2-related muscular dystrophycongenital muscular dystrophy type 1Alaminin alpha-2 deficiencymerosin-deficient congenital muscular dystrophymuscular dystrophy, congenital merosin-deficientmuscular dystrophy, congenital merosin-deficient, 1Amuscular dystrophy, congenital, due to partial LAMA2 deficiencymuscular dystrophy, congenital, merosin-deficient

Definition

Congenital muscular dystrophy type 1A (MCD1A) belongs to a group of neuromuscular disorders with onset at birth or infancy characterized by hypotonia, muscle weakness and muscle wasting.