(1994) Fetal hemoglobin synthesis in sickle cell anemia: Some molecular considerations. American Journal of Hematology 46 :10.1002/ajh.v46:2, 101-106 /Bhaumik K (1994). Fetal hemoglobin synthesis in sickle cell anemia: some molecular considerations. American Journal of Hematology, 46: 101-106....
An abnormal hemoglobin in which valine has replaced glutamic acid causing the hemoglobin to become less soluble under decreasing oxygen concentrations and to polymerize into crystals that distort the red blood cells into a sickle shape. Also called sickle cell hemoglobin. Pathophysiology Sickle-cell anae...
Anemia, Sickle CellThalassemiaAzacitidineFetal HemoglobinAmino AcidsStimulation, ChemicalAmino Acid SequenceMolecular Sequence DataPediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of diseases of children and disorders of development, extending from molecular biology ...
Fetal hemoglobin values with one exception were found elevated (> 2) in 89 patients with sickle-cell anemia and the mean level of Hb F was of 11.45 %. In 47 of these patients Hb F was more than 10 % by Singer's method. Hemoglobin and/or hematocrit val
The aim of our study was to characterise the global haemostatic potential of SS and AS adults. 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 ...
Sickle cell anemia and hemolytic anemia High-altitude living Taking an iron supplement Falsely high results An artificially high A1c test result can be caused by any of the following factors: Certain types of anemia, including iron-deficiency anemia ...
sickle cell disease phr. 镰状细胞病 sickle cell anemia 镰形(状)细胞性贫血,镰状细胞性贫血 sickle cell hemoglobin 镰刀形红细胞血红蛋白 sickle cell trait 镰形细胞(遗传)特性 sickle cell anaemia 镰刀状细胞(红血球)贫血 sickle cell hemoglobin D disease 镰状红细胞血红蛋白D病 sickle cell hemogl...
Examines developments in the study of the the molecular biology of sickle-cell anemia hemoglobin. Changing to the sickle-cell hemoglobin problem; Single AA mutation; Use of fingerprint technology to study other abnormal hemoglobins; Double mutants; Schema for the evolution of the hemoglobins; Treatme...
Sickle cells also have a shorter life span than normal red blood cells (10 to 20 days compared to 120 days). This rapid turnover may result in inadequate time to replace the red blood cells and may result in anemia. In sickle cell anemia, one defective hemoglobin gene is inherited from ...
Sickle cell anemia is a genetic disease where there is a problem with the protein hemoglobin. During sickle cell anemia people experience shortness of breath, dizziness, pale skin, headaches and fatigue. Answer and Explanation:1 Hemoglobin is low in sickle cell anemia because during this disease ...