Dilated cardiomyopathy due to dystrophinopathy (Q95450): Difference between revisions
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A cardiomiopatia dilatada por distrofinopatia é a presença de uma cardiomiopatia dilatada em associação com uma mutação da distrofina conhecida por estar associada a distrofia muscular. As distrofinopatias incluem distrofia muscular de Duchenne, distrofia muscular de Becker e cardiomiopatia dilatada ligada ao X. | |||
| description / en | description / en | ||
Dilated cardiomyopathy due to dystrophinopathy is the presence of a dilated cardiomyopathy in association with a dystrophin mutation known to be associated with muscular dystrophy. Dystrophinopathies include Duchenne muscular dystrophy, Becker muscular dystrophy and X-linked dilated cardiomyopathy. | |||
Revision as of 11:13, 16 August 2026
Dilated cardiomyopathy due to dystrophinopathy is the presence of a dilated cardiomyopathy in association with a dystrophin mutation known to be associated with muscular dystrophy. Dystrophinopathies include Duchenne muscular dystrophy, Becker muscular dystrophy and X-linked dilated cardiomyopathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1949109033 |
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| English | Dilated cardiomyopathy due to dystrophinopathy |
Dilated cardiomyopathy due to dystrophinopathy is the presence of a dilated cardiomyopathy in association with a dystrophin mutation known to be associated with muscular dystrophy. Dystrophinopathies include Duchenne muscular dystrophy, Becker muscular dystrophy and X-linked dilated cardiomyopathy. |
