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Up to: Congenital muscular dystrophy · LAMA2-related muscular dystrophy
Congenital merosin-deficient muscular dystrophy 1A
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.
This condition has no sub-types.