Shrinkage of Spleen in Sickle Cell Thalassemia: A rare case report
(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
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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
School of Public Health, Independent University, Bangladesh; Medical Officer, Department of Pediatrics, Anwer Khan Modern Medical College Hospital,Dhaka.
K Roy
Assistant Professor, Department of Pediatrics, Anwer Khan Modern Medical College Hospital, Dhaka
S Halder
Assistant Professor, Department of Pediatrics, Anwer Khan Modern Medical College Hospital, Dhaka
M Sheefa
Surveillance & Immunization Medical Officer, Dhaka North City Corporation, Bangladesh
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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