Autosomal recessive muscular dystrophy, childhood type, resembling Becker muscular dystrophy (Q93408): Difference between revisions
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A distrofia muscular autossômica recessiva infantil semelhante à doença de Becker é uma condição rara caracterizada por distrofia muscular com progressão leve do tipo Becker, afetando ambos os sexos igualmente. Refere-se a um grupo geneticamente heterogêneo de doenças nas quais diferentes defeitos moleculares e bioquímicos apresentam um fenótipo semelhante. A maioria dos pacientes possuem defeitos em um dos quatro genes do sarcoglicano identificados até o momento. | |||
| description / en | description / en | ||
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. | |||
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.
| Language | Label | Description | Also known as |
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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. |
