Catalog

Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia

No MMS code

Link to WHO Definition

Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia – http://id.who.int/icd/entity/160295890

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.