Congenital Muscular Dystrophies CMD

These are a type of muscular dystrophy. Don’t confuse these diseases with non-dystrophic congenital myopathies.

Merosin (Laminin 2) negative CMD:

Clinical features:

Cause hypotonia in the infant

Pathology, Muscle or skin biopsy:

H and E: dystrophic picture
Immunohistochemistry: absent Mersonin (Laminin 2) in basement membrane.

Findings on investigations:

MRI: white matter changes
 

Merosin positive CMD:

This is a group of diseases.
CMD with CNS malformations: a group of diseases. Merosin is positive.

Findings on investigations:

MRI: various CNS malformations
 

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