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Congenital merosin-deficient muscular dystrophy 1A
rareCongenital 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.
- Identifiers
- MONDO:0011925 OMIM:607855Orphanet:258
- Also known as
- CMD1A · congenital merosin-deficient muscular dystrophy type 1A · congenital muscular dystrophy caused by mutation in LAMA2 · congenital muscular dystrophy due to laminin alpha2 deficiency · LAMA2 congenital muscular dystrophy
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