Results 11 to 20 of about 11,856 (183)
Severe maternal morbidity according to sickle cell disease genotype
Background Sickle cell disease (SCD) is a genetic hemoglobinopathy that disproportionately affects individuals of African descent and is associated with elevated risks of maternal complications.
Tetsuya Kawakita +3 more
doaj +2 more sources
Sickle cells and sickle trait in thrombosis [PDF]
The blood cells form a beautiful and elegant system. For a century, hematologists have comfortably understood that each type of blood cell has its own independent function in immunity, hemostasis, or oxygen transport, but in this issue of Blood, Faes and colleagues show that nature is far more efficient than that.
openaire +2 more sources
Co-Inheritance of Sickle Cell Trait and Thalassemia Mutations in South Central Iran [PDF]
Background: We aimed to determine the incidence of co-inheritance as well as interaction of sickle cell trait (SCT) and αthal/βthal mutations in south and south central of Iran.
N Saleh-gohari, M Mohammadi-Anaie
doaj +1 more source
Sickle Cell Trait and Sudden Death
Sickle cell trait has long been considered a benign condition but continues to be the leading cause of death in young African Americans in military basic training and civilian organized sports.
Bruce L. Mitchell
doaj +1 more source
Prevalence of sickle cell disease and sickle cell trait in national neonatal screening studies
Sickle cell anemia is the best known hereditary blood disorder; there are serious complications associated with the condition. Diagnosis and early intervention reduce morbidity and mortality.
Luciana Garcia Lervolino +5 more
doaj +1 more source
A Unique Cause of Intestinal and Splenic Infarction in a Sickle Cell Trait Patient
Sickle-cell trait is a common genetic abnormality in the African American population. A sickle-cell crisis in a patient with sickle-cell trait is uncommon at best. Abdominal painful crises are typical of patients with sickle cell anemia.
Sofya H. Asfaw +5 more
doaj +1 more source
Background. To report a case of a pregnant woman with sickle cell trait (SCT) who presented with unilateral proliferative sickle cell retinopathy. Case Presentation.
Sepideh Ghods +7 more
doaj +1 more source
Sickle cell hemoglobin D disease First reported case in IRAN [PDF]
A case of sickle cell Hb D disease IS reported in young Iranian male. the father of whom carried an AS sickle cell trait and the mother an AD trait. This disease was diagnosed by Hb electrophoresis. agar gel electrophoresis sickling and solubility tests.
mohamad mehdi aflatouni, mohamad malek
doaj +1 more source
The genotype and phenotype correlation between coinheritance of heterozygous beta‐thalassemia with the alpha‐globin triplication is unclear. In this study we have investigated and reviewed alpha triplication frequency in beta‐thalassemia carriers, sickle
Mohammad Hamid +6 more
doaj +1 more source
The scope of clinical morbidity in sickle cell trait
Sickle cell trait (SCT), the heterozygous state of the sickle hemoglobin beta globin gene (HbAS) is carried by as many as 100 million individuals including up to 25% of the population in some regions of the World.
Azza A.G. Tantawy
doaj +1 more source

