Shrinkage of Spleen in Sickle Cell Thalassemia: A rare case report

F H Mone (1) , K Roy (2) , S Halder (3) , M Sheefa (4)
(1) School of Public Health, Independent University, Bangladesh; Medical Officer, Department of Pediatrics, Anwer Khan Modern Medical College Hospital,Dhaka. , Bangladesh
(2) Assistant Professor, Department of Pediatrics, Anwer Khan Modern Medical College Hospital, Dhaka , Bangladesh
(3) Assistant Professor, Department of Pediatrics, Anwer Khan Modern Medical College Hospital, Dhaka , Bangladesh
(4) Surveillance & Immunization Medical Officer, Dhaka North City Corporation, Bangladesh , Bangladesh

Abstract

The most prevalent monogenic gene disorder caused by defective hemoglobin in the blood is thalassemia. Splenectomy (Total/partial) is considered to be the alternative treatment method based on hypersplenism or iron overload and is an inherited-autosomal-recessive disorder. In South Asia, the far east, the Middle East, and Eastern Mediterranean nations, it is more prevalent. Over 40,000 children are born with Thalassemia every year.

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Authors

F H Mone
fabiamone@gmail.com (Primary Contact)
K Roy
S Halder
M Sheefa
Mone, F. H., Roy, K. ., Halder, S., & Sheefa, M. (2021). Shrinkage of Spleen in Sickle Cell Thalassemia: A rare case report. Jour Med Resh and Health Sci, 4(6), 1291–1293. https://doi.org/10.15520/jmrhs.v4i6.356
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