Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia (Q102550): Difference between revisions

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Latest revision as of 19:37, 16 August 2026

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
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.