Sharoff L. Enhancing Sickle Cell Anemia/Sickle Cell Disease Ge- netic Understanding through Simulation: A Descriptive Pilot Study. Journal of Nursing Education and Practice. 2015; 5(9): 39-48. http://dx.doi.org/10.5430/jnep.v5n9p39
6,12 Sickle cell anemia, in addition to causing a host of peripheral complications such as sickle cell crises, has been linked to cerebrovascular events. Strokes occur in 8 to 17 percent of patients with sickle cell anemia, although cerebral ischemic events usually do not occur in the context...
Incidence, demographic characteristics, and geographic distribution of sickle cell trait and sickle cell anemia births in Michigan, 1997–2014. Mol Genet Genomic Med. 2019;7(8). https://doi.org/10.1002/mgg3.795 Zempsky WT, Loiselle KA, McKay K, Lee BH, Hagstrom JN, Schechter NL. Do ...
用Quizlet學習並牢記包含What is sickle cell disease?、What causes sickle cell disease?、What are signs and symptoms of sickle cell anemia?等詞語及更多內容的單詞卡。
Sickle cell anemia; Children; Africa 1. Introduction Sickle cell disease (SCD) is a genetic blood disorder affecting red blood cells, with high morbidity and mortality rates. Sickle haemoglobin (HbS) is a structural variant of normal adult haemoglobin (HbA) (Chakravorty & Williams, 2015). SC...
Educators were unaware of the presence of students with sickle cell disease in the school, thus demonstrating the need for healtheducation actions to promote better care for these students.Key words: Anemia, Sickle Cell; Health Education; Students. 展开 ...
The most common and most severe form of SCD is the homozygous state known as Sickle Cell Anemia (SCA) due to inheritance of hemoglobin S (HbS) from each parent [1]. The inheritance of HbS in heterozygous state with a normal Hb is known as sickle cell trait which is not part of SCD ...
Olatokun WM (2010) Indigenous Knowledge of Traditional Medical practitioners in the treatment of sickle cell anemia. Indian J Traditional Knowledge 9(1):119–125 Google Scholar Oyebode O, Kandala NB, Chilton PJ, Lilford RJ (2016) Use of traditional medicine in middle-income countries: a WHO...
The median age of the patients was 30 years, and 81% of the patients had homozygous sickle cell anemia. Male patients outnumbered female patients during the first 2 years of the facility operation. During the last 3 years of the study, a nearly-equal distribution of the sexes was treated,...
cell anaemia, unspecified / Sickle cell anaemia / Anaemia sickle cell / Sickle-cell anaemia / Sickle cell disease NOS / Sickling disorder due to hemoglobin S (disorder) / Sickle-cell anemia / Sickle cell anemia / Sickle cell-hemoglobin SS disease (disorder) / Anemia sickle cell / Anemia, ...