Barth Syndrome is a rare but serious genetic disorder that affects males.
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Barth Syndrome Foundation
Promotes knowledge about this disease among families, physicians and scientists, serving as a focal point for data and research for scientists. The group offers support to families learning to cope with the disorder.
NINDS - Barth Syndrome Information
Information sheet compiled by the National Institute of Neurological Disorders and Stroke.
NORD: Barth Syndrome
Information on this rare, metabolic and neuromuscular genetic disorder provided by the National Organization for Rare Disorders.
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Last update:October 29, 2015 at 14:45:06 UTC