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IP International Journal of Medical Paediatrics and Oncology

Multiple endocrinopathies in β thalassemia major child – A case report

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Case Report

Author Details : Pottabathula Vinod kumar, B C. Yelamali*

Volume : 5, Issue : 1, Year : 2019

Article Page : 37-38

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Beta thalassemia is a chronic blood disorder characterised by decreased production of beta globin chains and excess accumulation of the other globin chains. Multiple endocrinopathies in β thalassemia major patients are common. Because of iron overload, multiple endocrinopathies are still prevalent despite extensive chelation therapy. Usuallylife expectancy may be increased by regular blood transfusions, butthere might begrowth problems, thyroid dysfunctions, hypoparathyroidism and hypocalcaemia. Here we are presentingaunusual case of various endocrinologicaldys functions in a chronic case of β thalassemia major.

Keywords: Hypoparathyroidism, Hypocalcaemia, β-Thalassemia major.

Doi : 10.18231/j.ijmpo.2019.007

How to cite : Kumar P V, Yelamali B C, Multiple endocrinopathies in β thalassemia major child – A case report. IP Int J Med Paediatr Oncol 2019;5(1):37-38

Copyright © 2019 by author(s) and IP Int J Med Paediatr Oncol. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (