Gilbert syndrome presenting in a young boy, confirmed by the rifampin test.
نویسندگان
چکیده
منابع مشابه
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 spherical, osmotically fragile erythrocytes that are selectively trapped by the spleen. The patients have...
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عنوان ژورنال:
- The Israel Medical Association journal : IMAJ
دوره 9 8 شماره
صفحات -
تاریخ انتشار 2007