Catalog

Centronuclear myopathy with type I fibre hypotrophy

No MMS code

Link to WHO Definition

Centronuclear myopathy with type I fibre hypotrophy – http://id.who.int/icd/entity/629192160

Autosomal dominant centronuclear myopathy (AD-CNM) is an inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy.