Barth Syndrome Foundation

  • 2005 Palmer Avenue
    Larchmont, NY 10538
  • 855-622-2784

Barth Syndrome is a series X-linked genetic disorder, primarily affecting males. It is caused by a mutation in the tafazzin gene resulting in an inborn error in lippid metabolism. The Barth Syndrome Foundation mission is to save lives through education, advances in treatment, and finding a cure for Barth syndrome.