Assessment of B2-Microglobulin Analysis for Renal Insufficiency in Iraqi β-Thalassemia Major Patients

Background: Beta-thalassemia is the most prevalent genetic hemoglobin apathy in the world. It is caused by a reduction or absence of beta-globin chain production, which is typically a portion of adult hemoglobin (HbA, which is α2β2). This genetic anomaly will lead to a rapid erythrocyte turnover, s...

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Bibliographic Details

Published in:	Al-Mustansiriyah Journal of Science
Main Authors:	Estabraq Salman Alwan, Thana Mohammed Juda, Liqaa M. Majed
Format:	Article
Language:	English
Published:	Mustansiriyah University 2024-09-01
Subjects:	β-thalassemia major B2-microglobulin Ferritin B.Urea Creatinine
Online Access:	https://mjs.uomustansiriyah.edu.iq/index.php/MJS/article/view/1391