Centronuclear myopathy (Q41397)
From determinar.ia.br - Determine suas informações
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C72.01 |
||
| English | Centronuclear myopathy |
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. |
Statements
CID11:8C72.01
0 references
