Dilated cardiomyopathy due to mucopolysaccharidoses (Q95459): Difference between revisions
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Cardiomiopatia dilatada devida a mucopolissacaridoses é a presença de cardiomiopatia dilatada em associação com o acúmulo lisossomal de glicosaminoglicanos (mucopolissacarídeos). Existem pelo menos 7 subtipos principais, com numerosas mutações associadas, com cardiomiopatia dilatada observada no Tipo I (síndrome de Hurler) e no Tipo VI (síndrome de Maroteaux-Lamy). | |||
| description / en | description / en | ||
Dilated cardiomyopathy due to mucopolysaccharidoses is the presence of dilated cardiomyopathy in association with the lysosomal accumulation of glycosaminoglycans (mucopolysaccharides). There are at least 7 main subtypes, with numerous associated mutations, with dilated cardiomyopathy noted in Type I (Hurler syndrome) and Type VI (Maroteaux-Lamy syndrome). | |||
Revision as of 11:14, 16 August 2026
Dilated cardiomyopathy due to mucopolysaccharidoses is the presence of dilated cardiomyopathy in association with the lysosomal accumulation of glycosaminoglycans (mucopolysaccharides). There are at least 7 main subtypes, with numerous associated mutations, with dilated cardiomyopathy noted in Type I (Hurler syndrome) and Type VI (Maroteaux-Lamy syndrome).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1767830504 |
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| English | Dilated cardiomyopathy due to mucopolysaccharidoses |
Dilated cardiomyopathy due to mucopolysaccharidoses is the presence of dilated cardiomyopathy in association with the lysosomal accumulation of glycosaminoglycans (mucopolysaccharides). There are at least 7 main subtypes, with numerous associated mutations, with dilated cardiomyopathy noted in Type I (Hurler syndrome) and Type VI (Maroteaux-Lamy syndrome). |
