Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia (Q102550)
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Hereditary inclusion body myopathy type 3 is characterised by congenital joint contractures (normalizing during early childhood), external ophthalmoplegia, and proximal muscle weakness. In adult cases, the muscular weakness is progressive.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_160295890 |
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| English | Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia |
Hereditary inclusion body myopathy type 3 is characterised by congenital joint contractures (normalizing during early childhood), external ophthalmoplegia, and proximal muscle weakness. In adult cases, the muscular weakness is progressive. |
Statements
CID11:ID_160295890
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