Early predictors of renal dysfunction in pediatric patients with sickle cell disease

Sickle cell disease (SCD) is a hereditary hemoglobinopathy characterized by abnormal hemoglobin production which leads to hemolytic anemia and intermittent occlusion of small blood vessels, which further leads to tissue ischemia, chronic organ damage, and organ dysfunction including urinary system....

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Bibliographic Details
Main Authors: Mohamed Abdelaziz El-Gamasy, Wageh S El-Naghy
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Indian Journal of Nephrology
Subjects:
Online Access:http://www.indianjnephrol.org/article.asp?issn=0971-4065;year=2019;volume=29;issue=1;spage=28;epage=33;aulast=El-Gamasy