A Comparative Study to Assess Parathyroid Hormone Status in Different Age Groups of b-Thalassaemia Major Individuals from Eastern India

Introduction: β-thalassaemia major, due to imbalance, missing or deficiency of β-globin chain synthesis pathway, is marked as a hereditary disorder. Homozygous state presents with severe anaemia. Regular blood transfusions and chelation therapy increase the life expectancy in thalassaemia patients....

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Bibliographic Details
Main Authors: Susmita Banerjee, Anindya Dasgupta
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2023-04-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://www.jcdr.net/articles/PDF/17728/62579_CE[Ra1]_F(IS)_PF1(DA_SS_KM)_PN(KM).pdf