(Q56014274)
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.
- Hereditary inclusion body myopathy type 3
- HIBM3
- IBM3
- Inclusion body myopathy type 3
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Identifiers
1 reference
1 reference