Hereditary inclusion body myopathy (Q88130): Difference between revisions

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Grupo de transtornos musculares raros com herança autossômica recessiva ou dominante e presença de fibras musculares com vacúolos marginados e agrupamento de túbulo-filamentos citoplasmáticos ou nucleares de 15-21 nm de diâmetro, conforme revelado por biópsia muscular. A forma mais comum de miopatia hereditária por corpúsculo de inclusão é devida a mutações no gene GNE que codifica uma enzima limitadora de taxa na via biossintética do ácido siálico. Isso resulta em sialilação anormal de glicoproteínas que possivelmente leva à degeneração da fibra muscular
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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

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
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ID_1248099703
    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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