A Rare Case of Compound Heterozygous Sickle Cell Beta Thalassaemia with High HbF and Normal HbA2 Levels Detected on HPLC

Compound heterozygous Sickle Haemoglobin (HbS) beta (β) thalassaemia arises from the mutations associated with sickle cell and β thalassaemia and significantly affects populations in low income countries like India. Elevated levels of Haemoglobin A2 (HbA2) represent the primary indicator for identif...

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Bibliographic Details

Published in:	Journal of Clinical and Diagnostic Research
Main Authors:	Ruchi Agarwal, Sunaina Hooda, parul, Kulwant Singh, Adesh Thombre
Format:	Article
Language:	English
Published:	JCDR Research and Publications Private Limited 2024-05-01
Subjects:	compound heterozygous sickle cell β thalassaemia foetal haemoglobin haemoglobin a2 haemolytic anaemia high performance liquid chromatography sickling
Online Access:	https://jcdr.net/articles/PDF/19436/69437_CE[Ra1]_F(IS)_PF1(KB_DK_OM)_redo_Ref_Pat(OM)_PFA(SS)_PB(KB_OM)_PN(OM).pdf