Barth Syndrome Treatment Market is driven by rising prevalence of Barth syndrome

Barth syndrome is a rare genetic disorder characterized by muscle weakness,delayed growth, fatigue with exercise and enlarged heart or cardiomyopathy. Barth syndrome affects mostly males and symptoms often begin in infancy or early childhood. The exact prevalence is unknown but it is estimated that Barth syndrome affects1in 300,000 to 400,000 newborn males. Treatment focuses onmanaging symptoms and treating associated medical problems.

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