Autosomal recessive muscular dystrophy, childhood type, resembling Becker muscular dystrophy (Q93408): Difference between revisions
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CID11:ID_391677057 | |||||||||||||||
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dki-india-ID_391677057 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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Latest revision as of 08:30, 16 August 2026
Childhood autosomal recessive muscular dystrophy resembling Becker disease is a rare condition characterised by muscular dystrophy with mild, Becker-like progression, affecting both sexes equally. It refers to a genetically heterogeneous group of disorders in which different molecular and biochemical defects present with a similar phenotype. Most patients have defects in one of the four sarcoglycan genes identified to date.
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| default for all languages | ID_391677057 |
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| English | Autosomal recessive muscular dystrophy, childhood type, resembling Becker muscular dystrophy |
Childhood autosomal recessive muscular dystrophy resembling Becker disease is a rare condition characterised by muscular dystrophy with mild, Becker-like progression, affecting both sexes equally. It refers to a genetically heterogeneous group of disorders in which different molecular and biochemical defects present with a similar phenotype. Most patients have defects in one of the four sarcoglycan genes identified to date. |
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CID11:ID_391677057
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dki-india-ID_391677057
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Concluído
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15 August 2026
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