A Rare Case of Coexistence of Homozygous β-Thalassaemia and Glucose 6 Phosphate Dehydrogenase Deficiency

A Rare Case of Coexistence of Homozygous β-Thalassaemia and Glucose 6 Phosphate Dehydrogenase Deficiency

β-thalassaemia is one of the most prevalent autosomal disorders worldwide. Mutations/deletions in globin gene underlie deficiencies in Haemoglobin (Hb) production, which can interfere with oxygen delivery by Hb, resulting in thalassaemias causing anaemias with a wide range of disease severity. Glu...

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Bibliographic Details
Main Authors: Jitendar Mohan Khunger, Monika Gupta, Ankur Jain, Monica Khunger Malhotra
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2020-10-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
anaemia
haemoglobin
pallor
red blood cells
Online Access:https://jcdr.net/articles/PDF/14085/44968_CE[Ra1]_F(SL)_PF1(AG_KM)_PFA_NC(KM)_PN(SL).pdf

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