Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia (Q102550): Difference between revisions
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Miopatia por corpúsculo de inclusão hereditária tipo 3 é caracterizada por contraturas articulares congênitas (que se normalizam durante a primeira infância), oftalmoplegia externa e fraqueza muscular proximal. Nos pacientes adultos, a fraqueza muscular é progressiva. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
