hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome (Q56014274)
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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.
- Hereditary inclusion body myopathy type 3
- HIBM3
- IBM3
- Inclusion body myopathy type 3
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome |
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. |
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1 reference
1 reference