Sickle Cell Trait and Hemoglobin C Trait说明书
Conclusion: Black children with sickle cell trait or hemoglobin C trait have an increased risk of invasive pneumococcal disease. 展开 关键词: Humans Streptococcus pneumoniae Pneumococcal Infections Sickle Cell Trait Hemoglobin C Population Surveillance Child, Preschool Infant, Newborn Infant Risk Factors ...
N. M. Nseka心血管病(英文)Lepira FB, Mukendi TK, Mbutiwi FIN, Makulo JR, Sumaili EK, Kayembe PK, et al. Sickle cell trait, hemoglobin levels and anemia among black patients with predialysis chronic kidney disease: a post hoc analysis. World J Cardiovasc Dis. 2016;6:258....
Patients with sickle cell trait may experience mild if any, symptoms at all. In sickle cell disease, symptoms are more significant, especially in episodes of acute crisis. These symptoms can include: Generalized body aches and pain Chest pain Bone pain Shortness of breath Ulceration of the ...
Materials and Methods: Three groups were studied and consisted in 31 controls (group AA), 26 sickle cell trait (group AS) and 29 SCD patients (group SS) at steady state. Hemoglobin phenotype was assessed by combination of cation-exchange high performance chromatography (beta-thal short program ...
Sickle cell hemoglobin S (HbS) and hemoglobin C (HbC) are structural variants of β-globin that differ from each other by a single amino acid residue.1α-Thalassemias result from an impaired production of α-globin, whereby α+- and α0-forms are caused by deletions that leave 1 functiona...
Although several other hemoglobins (including C, E, O, and D) are eluted with HbA2, it is unlikely that one of these hemoglobins would be present in a person being tested for elevated HbA2. HbA2 measurement is used in the diagnosis of β-thalassemia trait, in which the HbA2 is ...
Fasting plasma glucose (FPG) and hemoglobin A1c (HbA1c) are both used to diagnose diabetes, but these measurements can identify different people as having diabetes. We used data from 117 population-based studies and quantified, in different world regions
In this example, patients with normal red cells, sickle-cell disease red cells, and sickle-cell trait red cells can be distinguished on a per cell basis from patients with sickle-cell anemia who are transfused and thus have a population of SS red cells and AA red cells, which cann...
We mapped quantitative trait loci (QTLs) influencing red cell hydration using the cell hemoglobin concentration mean (CHCM) as a marker of hydration status. CHCM (analogous to the calculated mean cell hemoglobin content, MCHC) was obtained using an Advia 120 whole blood analyzer, which provides a...