Assessment of Iron Overload in Homozygous and Heterozygous Beta Thalassemic Children below 5 Years of Age

Background: Thalassemia is a genetic disease having 3-7% carrier rate in Indians. It is transfusion dependent anemia having high risk of iron overloading. A clinical symptom of iron overload becomes detectable in second decade causing progressive liver, heart and endocrine glands damage. There...

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Bibliographic Details
Main Authors: Dhiraj J. Trivedi, Aparna Sagare
Format: Article
Language:English
Published: Krishna Institute of Medical Sciences University 2014-07-01
Series:Journal of Krishna Institute of Medical Sciences University
Subjects:
Online Access:http://www.jkimsu.com/jkimsu-vol3no2/JKIMSU,%20Vol.%203,%20No.%202,%20July-Dec%202014%20Page%2017-22.pdf