Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
What is 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.
Other condition names
- HIBM3
- Hereditary inclusion body myopathy type 3
- IBM3
- Inclusion body myopathy type 3
Inheritance type
Autosomal dominant
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Adolescent
- Infancy
- Neonatal
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