Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?

被引：0

作者：

Prashant Warang

Rati Devendra

Selma D’Silva

Ashish Chiddarwar

Prabhakar Kedar

Kanjaksha Ghosh

Roshan Colah

Malay B. Mukherjee

机构：

[1] National Institute of Immunohaematology,Department of Haematogenetics

[2] Indian Council of Medical Research,undefined

来源：

Annals of Hematology | 2015年 / 94卷

关键词：

Promoter Polymorphism; Biliverdin; Serum Bilirubin Level; Osmotic Fragility; Hereditary Spherocytosis;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：169 / 171

页数：2

共 26 条

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[2]

Gallagher PG(2012)Guidelines for the diagnosis and management of hereditary spherocytosis—2011 update Br J Haematol 156 37-49

[3]

Mohandas N(1999)Coinheritance of Gilberts syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis Blood 94 2259-2262

[4]

Bolton-Maggs PH(2008)Hereditary spherocytosis coexisting with Gilbert’s syndrome: a diagnostic dilemma Singapore Med J 49 308-309

[5]

Langer JC(2012)Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis J Pediatr Hematol Oncol 34 54-56

[6]

Iolascon A(2011)Flow cytometric osmotic fragility—an effective screening approach for red cell membranopathies Cytometry B Clin Cytom 80 186-190

[7]

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[8]

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[9]

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[10]

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