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

Mone, F., Roy, K., Halder, S. and Sheefa, M. 2021. Shrinkage of Spleen in Sickle Cell Thalassemia: A rare case report. Journal of Medical Research and Health Sciences. 4 (6), pp. 1291-1293. https://doi.org/10.15520/jmrhs.v4i6.356

TitleShrinkage of Spleen in Sickle Cell Thalassemia: A rare case report
TypeJournal article
AuthorsMone, F., Roy, K., Halder, S. and Sheefa, M.
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.

JournalJournal of Medical Research and Health Sciences
Journal citation4 (6), pp. 1291-1293
ISSN2589-9023
2589-9031
Year2021
PublisherMRERP LTD.
Publisher's version
License
CC BY-NC-ND 4.0
File Access Level
Open (open metadata and files)
Digital Object Identifier (DOI)https://doi.org/10.15520/jmrhs.v4i6.356
Web address (URL)https://jmrhs.info/index.php/jmrhs/article/view/356
Publication dates
Published21 Jun 2021

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