Hereditary inclusion body myopathy (Q88130): Difference between revisions
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13 August 2026
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Latest revision as of 14:15, 15 August 2026
Group of rare muscle disorders with autosomal recessive or dominant inheritance and presence of muscle fibres with rimmed vacuoles and collection of cytoplasmic or nuclear 15-21 nm diameter tubulo-filaments as revealed by muscle biopsy. The most common form of hereditary inclusion-body myopathy is due to mutations of the GNE gene that codes for a rate-limiting enzyme in the sialic acid biosynthetic pathway. This results in abnormal sialylation of glycoproteins that possibly leads to muscle fibre degeneration
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1248099703 |
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| English | Hereditary inclusion body myopathy |
Group of rare muscle disorders with autosomal recessive or dominant inheritance and presence of muscle fibres with rimmed vacuoles and collection of cytoplasmic or nuclear 15-21 nm diameter tubulo-filaments as revealed by muscle biopsy. The most common form of hereditary inclusion-body myopathy is due to mutations of the GNE gene that codes for a rate-limiting enzyme in the sialic acid biosynthetic pathway. This results in abnormal sialylation of glycoproteins that possibly leads to muscle fibre degeneration |
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CID11:ID_1248099703
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dki-india-ID_1248099703
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Concluído
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13 August 2026
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