Central core disease (Q41401)
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Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental delay) and is characterised by predominantly proximal weakness, pronounced in the hip girdle.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C72.02 |
||
| English | Central core disease |
Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental delay) and is characterised by predominantly proximal weakness, pronounced in the hip girdle. |
Statements
CID11:8C72.02
0 references
dki-india-8C72.02
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