Haematological values in Homozygous Sickle Cell Disease in Steady State and Haemoglobin Phenotypes AA Controls in Lagos, Nigeria.

Background: Sickle cell disease is a genetic abnormality involving the haemoglobin. The consequent haemoglobin S causes polymerization of haemoglobin resulting in haemolysis and anaemia. Although, it is primarily a red cell disorders, the white blood cells and platelets are also affected by the muta...

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Bibliographic Details
Main Authors: Akinsegun Akinbami, Adedoyin Dosunmu, Adewumi Adediran, Olajumoke Oshinaike, Phillip Adebola, Vincent Osunkalu, Olanrewaju Arogundade, Oluwaseun Adelekan
Format: Article
Language:English
Published: PAGEPress Publications 2014-08-01
Series:Mediterranean Journal of Hematology and Infectious Diseases
Subjects:
Online Access:https://mjhid.org/index.php/mjhid/article/view/1703