Complete Information on Barth syndrome
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Barth syndrome also known as 3-Methylglutaconic aciduria type II. Barth syndrome is a rare, metabolic, and neuromuscular, genetic disorder that occurs particularly in males, since it is passed from mother to son through the X chromosome. Signs and symptoms of Barth syndrome including metabolism distortion, delayed motor skills, stamina deficiency, hypotonia, chronic fatigue, delayed growth, cardiomyopathy, and compromised immune system. Some of the symptoms may be transitory, although in some individuals, symptoms can be severe, and the disorder may be lethal.
