Abstract
Congenital muscular dystrophies are autosomal recessive inherited disorders. There are two categories depending on the structural involvement of the central nervous system. The classic form of congenital muscular dystrophy can be subdivided into two groups the merosin-negative and merosin-positive.
We describe the case of a patient with severe hypotonia, joint contractures and white matter changes in the central nervous system, the authors considered to be a case of merosindeficient congenital muscular dystrophy.
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