Possible role of hemoglobin S in implicating hemostatic and inflammatory reactions: Study on Saudi Arabian population

Background: Sickle cell disease (SS), is one of the most common inherited hematologic disorders, presents with chronic hemolytic anemia that can be punctuated by crises, infarcts, organ damage and hypercoagulable state. Sickle cell trait (AS) is a benign disorder. However, there is an increased risk...

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Bibliographic Details
Main Authors: Mohammed A Sorour, Salwa A Dabbous, Reham Abdel Aleem Mohamed Afify
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Journal of Applied Hematology
Subjects:
Online Access:http://www.jahjournal.org/article.asp?issn=1658-5127;year=2015;volume=6;issue=2;spage=64;epage=69;aulast=Sorour