Extreme hyperbilirubinemia: An indicator of morbidity and mortality in sickle cell disease

doi:10.4254/wjh.v11.i3.287

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World Journal of Hepatology

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1948-5182

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Retrospective Cohort Study

World J Hepatol. Mar 27, 2019; 11(3): 287-293
Published online Mar 27, 2019. doi: 10.4254/wjh.v11.i3.287

Table 3 Hemoglobin genotype breakdown between the extreme hyperbilirubinemia and control groups

	Hemoglobin SS (n)	Hemoglobin S Beta+ Thalassemia (n)	Hemoglobin S Beta null Thalassemia (n)	Hemoglobin S Beta (unknown) Thalassemia (n)	Hemoglobin SC (n)
Extreme hyperbilirubinemia	40	2	0	0	0
Control	33	11	2	2	51

EH: Extreme hyperbilirubinemia.

Citation: Haydek JP, Taborda C, Shah R, Reshamwala PA, McLemore ML, Rassi FE, Chawla S. Extreme hyperbilirubinemia: An indicator of morbidity and mortality in sickle cell disease. World J Hepatol 2019; 11(3): 287-293
URL: https://www.wjgnet.com/1948-5182/full/v11/i3/287.htm
DOI: https://dx.doi.org/10.4254/wjh.v11.i3.287