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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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| Izdano u: | Pediatr Gastroenterol Hepatol Nutr |
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| Glavni autori: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4291453/ https://ncbi.nlm.nih.gov/pubmed/25587528 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5223/pghn.2014.17.4.266 |
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