3-methylglutaconic aciduria type 5 (Q101481): Difference between revisions
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A cardiomiopatia dilatada com ataxia (DCMA) é caracterizada por início precoce grave (antes dos três anos de idade) cardiomiopatia dilatada com defeitos de condução (síndrome do QT longo), ataxia cerebelar não progressiva, disgenesia testicular e acidúria 3-metilglutacônica. | |||
| description / en | description / en | ||
Dilated cardiomyopathy with ataxia (DCMA) is characterised by severe early onset (before the age of three years) dilated cardiomyopathy (DCM) with conduction defects (long QT syndrome), non-progressive cerebellar ataxia, testicular dysgenesis, and 3-methylglutaconic aciduria. | |||
Revision as of 18:17, 16 August 2026
Dilated cardiomyopathy with ataxia (DCMA) is characterised by severe early onset (before the age of three years) dilated cardiomyopathy (DCM) with conduction defects (long QT syndrome), non-progressive cerebellar ataxia, testicular dysgenesis, and 3-methylglutaconic aciduria.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_422277813 |
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| English | 3-methylglutaconic aciduria type 5 |
Dilated cardiomyopathy with ataxia (DCMA) is characterised by severe early onset (before the age of three years) dilated cardiomyopathy (DCM) with conduction defects (long QT syndrome), non-progressive cerebellar ataxia, testicular dysgenesis, and 3-methylglutaconic aciduria. |
