An Uncommon Display of the Sickle Cell Trait Coupled with the Beta-Thalassemia Trait as Hypersplenism

A structural flaw in the globin gene causes hemoglobinopathies, while a flaw in the globin chain’s synthesis causes thalassemia. One of the most prevalent hemoglobinopathies worldwide is sickle cell disease. Any region of the body can be affected, but the spleen is one of the most often afflicted an...

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Bibliographic Details

Published in:	Journal of Integrated Health Sciences
Main Authors:	Divyesh Patel, Vedangi Desai, Palak Doshi, Shubham R. Darda, Jitendra D. Lakhani
Format:	Article
Language:	English
Published:	Wolters Kluwer – Medknow Publications 2023-07-01
Subjects:	hypersplenism sickle cell trait thalassemia trait
Online Access:	https://journals.lww.com/10.4103/jihs.jihs_46_23