Coexistence of Gilbert Syndrome and Hereditary Spherocytosis in a Child Presenting with Extreme Jaundice

Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. It is characterized by intermittent episodes of jaundice in the absence of hepatocellular disease or hemolysis. Hereditary spherocytosis is the most common inherited hemolytic anemia and is characterized by spherica...

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Detalles Bibliográficos
Autores principales: Lee, Jae Hee, Moon, Kyung Rye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4291453/
https://www.ncbi.nlm.nih.gov/pubmed/25587528
http://dx.doi.org/10.5223/pghn.2014.17.4.266

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4291453/
https://www.ncbi.nlm.nih.gov/pubmed/25587528
http://dx.doi.org/10.5223/pghn.2014.17.4.266

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