What is Merosin Deficient Congenital Muscular Dystrophy (CMD)?
Merosin Deficient Congenital Muscular Dystrophy (CMD) is a rare genetic disorder affecting newborns, characterized by muscle weakness and dystrophy. This condition is caused by mutations in the LAMA2 gene, which leads to a deficiency of merosin, a crucial protein for muscle and nerve function.
