Tag: cardiomyopathy
Barth syndrome: A potential treatment for a rare disease
Barth syndrome is a rare disorder in males caused by a variant of the gene TAFAZZIN. It affects the metabolism of the fat molecule cardiolipin in mitochondria, resulting in the dysfunction of skeletal muscle and the heart. The syndrome doesn’t have a specific therapy, so patients who suffer from it have health problems their entire lives and are more likely […]
Read More… from Barth syndrome: A potential treatment for a rare disease