The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.

BACKGROUND: Co-inheritance of α-thalassemia was reported to be associated with a delayed age of disease onset among Cameroonian Sickle Cell Anemia (SCA) patients. The present study aimed to explore the correlation between α-thalassemia, hematological indices, and clinical events in these patients. M...

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Bibliographic Details
Main Authors: Maryam Bibi Rumaney, Valentina Josiane Ngo Bitoungui, Anna Alvera Vorster, Raj Ramesar, Andre Pascal Kengne, Jeanne Ngogang, Ambroise Wonkam
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4076272?pdf=render