@article{ajmcr2017575,
author={{S., Dhayhi Nabil and M., Arishi Haider and Y., Alnami Mohammed and Prabhara, Dammur},
title={Visceral Leishmaniasis with Secondary Hemophagocytosis in a Sickle Cell Anemia Patient},
journal={American Journal of Medical Case Reports},
volume={5},
number={7},
pages={187--189},
year={2017},
url={http://pubs.sciepub.com/ajmcr/5/7/5},
issn={2374-216X},
abstract={Sickle cell anemia (SCA ) is one of the most common hemoglobinopathies, which is characterized by a high level of abnormal hemoglobin called hemoglobin S (Hb S). This abnormal hemoglobin results from changes in amino acids and valine instead of glutamine at the sixth position of the ¦Â globin molecule. Two affected genes are needed to develop sickle cell anemia, homozygous Hb S.},
doi={10.12691/ajmcr-5-7-5}
publisher={Science and Education Publishing}
}