219 top medical experts on Triple X syndrome across 35 countries and 20 U.S. states, including 68 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Triple X syndrome: A form of Crigler Najjar syndrome (CNS), a hereditary disorder of hepatic bilirubin conjugation, characterized by severe neonatal unconjugated hyperbilirubinemia due to a complete absence of hepatic UDP-glucuronosyltransferase 1A1. The disorder clinically manifests with neonatal, isolated, severe and permanent jaundice with a permanent risk of bilirubin encephalopathy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Organizations Providing General Support

  • Synonyms: 47,XXX syndrome,  47,Xxx,  Super female,  Triple-X chromosome syndrome,  Triple-X female,  Triplo X syndrome,  Trisomy X,  XXX syndrome


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