eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | cardiomyopathy |
| Comorbidity | C0574083|barth syndrome |
| Sentences | 4 |
| PubMedID- 23031367 | Intrafamilial variability for novel taz gene mutation: barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle. |
| PubMedID- 22427193 | barth syndrome (bths) is associated with myocardial disease, frequently left ventricular noncompaction cardiomyopathy, which may necessitate cardiac transplantation or lead to death in some patients. |
| PubMedID- 24116962 | The first disorder linked to abnormal mitochondrial lipid metabolism was barth syndrome of dilated cardiomyopathy associated with cyclical neutropenia, growth retardation and 3-methylglutaconic aciduria (clarke et al., 2013). |
| PubMedID- 20812380 | barth syndrome: an x-linked cause of fetal cardiomyopathy and stillbirth. |
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