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PedAM

Pediatric Disease Annotations & Medicines




Disease cardiomyopathy
Phenotype C0574083|barth syndrome
Sentences 4
PubMedID- 20812380 barth syndrome: an x-linked cause of fetal cardiomyopathy and stillbirth.
PubMedID- 22427193 Left ventricular noncompaction cardiomyopathy in barth syndrome: an example of an undulating cardiac phenotype necessitating mechanical circulatory support as a bridge to transplantation.
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- 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).

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