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吉尔伯特综合征加重了一名遗传性球形红细胞增多症患儿的非结合性高胆红素血症。

Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.

作者信息

Kumar Dipti, Parakh Ankit, Sharma Sunita

机构信息

Department of Pediatrics, Lady Hardinge Medical College and Kalawati Saran Children's Hospital, New Delhi, India.

出版信息

J Pediatr Hematol Oncol. 2012 Jan;34(1):54-6. doi: 10.1097/MPH.0b013e318228fdd1.

Abstract

Hemolytic anemia usually gives rise to only a modest elevation of serum bilirubin. Unconjugated hyperbilirubinemia of an extreme degree should raise suspicion of additional factors. We describe a 10-year-old child suffering from hereditary spherocytosis, who had unusually high levels of unconjugated serum bilirubin and was diagnosed to have Gilbert syndrome on the basis of genetic analysis.

摘要

溶血性贫血通常只会引起血清胆红素适度升高。极度的非结合性高胆红素血症应引发对其他因素的怀疑。我们描述了一名患有遗传性球形红细胞增多症的10岁儿童,其非结合性血清胆红素水平异常高,并根据基因分析被诊断为吉尔伯特综合征。

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