236 top medical experts on Barth Syndrome across 21 countries and 23 U.S. states, including 75 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Barth Syndrome: Rare congenital X-linked disorder of lipid metabolism. Barth syndrome is transmitted in an X-linked recessive pattern. The syndrome is characterized by muscular weakness, growth retardation, dilated cardiomyopathy, variable neutropenia, 3-methylglutaconic aciduria (type II) and decreases in mitochondrial cardiolipin level. Other biochemical and morphological mitochondrial abnormalities also exist.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Congenital Heart Defects (4,797), Multiple Abnormalities (3,208), X-Linked Genetic Diseases (2,304), Inborn Errors Lipid Metabolism (797).
  4. Clinical Trials ClinicalTrials.gov : at least 6 including 4 Completed


  

        

                    


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