Centronuclear myopathy (Q41397)
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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
dki-india-8C72.01
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