Laminin subunit alpha 2-related congenital muscular dystrophy

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Name:
Laminin subunit alpha 2-related congenital muscular dystrophy
Description:
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.
ORPHAcode:
258
Synonyms:
CMD1A
Congenital muscular dystrophy due to laminin alpha2 deficiency
Congenital muscular dystrophy type 1A
MDC1A
Merosin-negative congenital muscular dystrophy
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14