Do you look for 'literature review of sickle cell anemia'? Here you can find questions and answers on the topic.
Letter a review of the literature was conducted to identify better practices regarding bother management in adolescents with sickle cadre anemia. Key speech such as pain in the ass, pain management, immature sickle cell anaemia, and acute reaping hook cell pain were entered into databases to reveal analysis and quantitative studies from 2009 to the present.Author: Bridget H. Wilson, Jessica NelsonCited by: Put out Year: 2015
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- Literature review of sickle cell anemia in 2021
- Sickle cell anemia news, articles
- Sickle cell journal articles
- Exercise and sickle cell anemia
- Research paper on sickle cell anemia
- Review article sickle cell disease
- Research topics on sickle cell disease
- Google scholar
Literature review of sickle cell anemia in 2021
Sickle cell anemia news, articles
Sickle cell journal articles
Exercise and sickle cell anemia
Research paper on sickle cell anemia
Review article sickle cell disease
Research topics on sickle cell disease
Google scholar
What happens if Sickle Cell Anemia is left untreated?
One of the most common is sickle cell anemia, which, due to sickling of erythrocytes, causes vaso-occlusive phenomena. Among the possible ocular manifestations, the most representative is retinopathy, which can lead to blindness if left untreated.
How does low oxygen tension cause sickle cell disease?
In sickle cell disease, low oxygen tension promotes red blood cell sickling and repeated episodes of sickling damage the cell membrane and decreases the cell's elasticity. These cells fail to return to normal shape when normal oxygen tension is restored.
How does sickle cell disease affect quality of life?
[…] Sickle cell disease (SCD) is a chronic condition associated with high mortality and morbidity. It is characterized by acute clinical symptoms such as painful vaso-occlusive crises, which can impair health-related quality of life (HRQL).
What causes sickle cell anaemia in red blood cells?
The association of two mutant β-globin subunits forms haemoglobin S (HbS). Under low-oxygen conditions, the absence of a polar amino acid at position of six of the β-globin chain promotes the non-covalent polymerization of haemoglobin, which distorts red blood cells into a sickle shape and decreases their elasticity.
Last Update: Oct 2021