Pubertal Development in Girls with Beta Thalassaemia and Assessment of the Adequacy of Chelation Therapy: A Quasi-experimental Study

Introduction: Beta thalassaemia is the most prevalent hereditary autosomal disorder, significantly impacting endocrine function during pubertal development. The pathology is rooted in the excessive deposition of iron in vital organs. If left untreated, this condition leads to serious morbidity and m...

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Bibliographic Details
Main Authors: Rupali Modak, Amitava Pal, Shuvendu Das, Dilip Kumar Biswas
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2024-03-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://www.jcdr.net/articles/PDF/19165/64430_CE[Ra1]_F(SL)_Ref_PAT(SL)_QC(SHK_IS))_PF1(RI_DK_OM)_PFA(RI_KM)_PN(KM).pdf