Sickle ß-globin haplotypes among patients with sickle cell anemia in Basra, Iraq: A cross-sectional study
BACKGROUND: Sickle cell disease is a monogenic disease with heterogeneous clinical course. Many genetic factors such as inheritance of α-thalassemia trait and fetal hemoglobin (Hb) level, related to the presence of specific haplotypes, are among the factors that modify disease severity. OBJECTIVES:...
Main Authors: | Noor Taha Yaseen, Hind Shaker Al-Mamoori, Mea`ad Kadhum Hassan |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2020-01-01
|
Series: | Iraqi Journal of Hematology |
Subjects: | |
Online Access: | http://www.ijhonline.org/article.asp?issn=2072-8069;year=2020;volume=9;issue=1;spage=23;epage=29;aulast=Yaseen |
Similar Items
-
Coagulation activation in patients with sickle cell disease in Basra, Iraq
by: Wasan H Saud, et al.
Published: (2017-01-01) -
Prevalence of hepatitis C virus seropositivity among multitransfused patients with hereditary anemias in Basra, Iraq
by: Oula Abdullah Najim, et al.
Published: (2018-01-01) -
The frequency of βS-globin haplotypes in the state of Paraná, Brazil, and clinical manifestations of sickle cell anemia
by: Alexandra M. Watanabe, et al. -
School performance of children with sickle cell disease in Basra, Iraq
by: Falah Hassan Abid, et al.
Published: (2019-01-01) -
Influence of ?S-globin haplotypes and hydroxyurea on tumor necrosis factor-alpha levels in sickle cell anemia
by: Marília Rocha Laurentino, et al.
Published: (2014-04-01)