Catalog

Centronuclear myopathy

8C72.01

Link to WHO Definition

Centronuclear myopathy – http://id.who.int/icd/entity/742097637

Centronuclear myopathy (CNM) is an inherited neuromuscular disorder characterised by clinical features of a congenital myopathy and centrally placed nuclei on muscle biopsy. It encompasses the X-linked form, the autosomal recessive form and the autosomal dominant form with a highly variable clinical presentation.

Parents

Children