212 top medical experts on Crigler-Najjar Syndrome across 30 countries and 7 U.S. states, including 50 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Crigler-Najjar Syndrome: A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Hereditary Hyperbilirubinemia (123).
- Clinical Trials : at least 11 including 5 Completed, 2 Recruiting
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