Sickle Cell Trait and Hemoglobin C Trait说明书
Sickle cellPatients with sickle cell disease commonly experience painless hematuria. Hematuria may be found in patients with sickle cell trait, sickle cell anemia, and sickle cell hemoglobin C disease, but it is believed to be uncommon in patients with other hemoglobinopathies, such as hemoglobin ...
Blacks with sickle cell trait or hemoglobin C trait had 77% (95% CI = 22-155) and 42% (95% CI = 1-100) higher rates than whites and blacks with normal hemoglobin. Conclusion: Black children with sickle cell trait or hemoglobin C trait have an increased risk of invasive pneumococcal ...
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 ...
英文: In the United States, hemoglobin S and C traits are carried by 7.8% and 2.3% of African Americans, respectively, and 0.8% carry the beta-thalassemia trait (2).中文: 在美国,美籍非洲人血红蛋白S和C的携带率分别为7.8%和2.3%,β地中海贫血的携带率为0.8%。
Synonym(s):sickle cell hemoglobin,haemoglobin S. Medical Dictionary for the Health Professions and Nursing © Farlex 2012 Hemoglobin S Hemoglobin produced in association with the sickle cell trait; the beta-globin molecules of hemoglobin S are defective. ...
In sickle-cell anemic infants, the proportion of abnormal hemoglobin rises to near-adult levels by 6 months of age. After 6 months of age, the sickling of RBCs is a constant finding. In individuals with the sickle cell trait, the proportion of Hb S is between 35% and 45%. Of course...
ATN Tita,JR Biggio,V Chapman,C Neely,DJ Rouse 摘要: OBJECTIVE: Recent studies have reported increased fetal loss and preeclampsia in women with sickle cell trait (hemoglobin [Hb] AS). There is a paucity of studies of outcomes in carriers of hemoglobin C. We examined the prevalence of ...
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 ...
Hematology and coagulation Zane D. Amenhotep, in Self-Assessment Q&A in Clinical Laboratory Science, III, 2021 What is the best interpretation of the hemoglobin gel electrophoresis? a. hemoglobin S trait b. hemoglobin S disease c. hemoglobin C trait d. hemoglobin C disease e. hemoglobin SC dis...