Sickle Cell Anemia - Essay Example

Thalassemia and Sickle Cell Anemia are considered sub-sets of hemolytic anemia (Vorvick, Chen, & Zieve, 2010) Fatigue; episodic pain in the bones, joints, and Anemia Types Causes Symptoms Diagnosis Treatment Iron Deficiency Anemia Insufficient iron in the diet; blood loss; inability to properly absorb iron;pregnancy (Mayo Clinic staff, 2011e)Unusual fatigue and weakness; paleness; headache; dizziness, lightheadedness, and vertigo; irritability; poor appetite; restless leg syndromeInitial symptoms may be so mild as to be unnoticeable(Mayo Clinic staff, 2011f)Blood tests to visually look for small, pale red blood cellsHemocrit, hemoglobin, and ferritin testingTests to determine initial cause of anemia(Mayo Clinic staff, 2011g)Use of oral iron supplementationTreatment of underlying cause of blood loss, such as peptic ulcersMany times treatment is preventative, such as giving iron tablets to women who have heavy menstrual bleeding or are pregnant(Mayo Clinic staff, 2011h)Vitamin Deficiency AnemiaLack of vitamins required to create healthy blood cells, either from a lack of those nutrients in the diet or from an inability to properly absorb those nutrients (Mayo Clinic staff, 2011i)Fatigue; mental status changes; yellowish or pale skin; muscle weakness and loss of balance; swollen, dark red tongue; diarrhea; unintentional weight loss; numbness or tingling sensation (Mayo Clinic staff, 2011j)Blood tests to visually confirm smaller and fewer red blood cellsLevels of certain vitamins (namely, folate, B-12, and Vitamin C) in the bloodstreamTests to determine initial cause of vitamin deficiency(Mayo Clinic staff, 2011k)Treatment for vitamin deficiency anemia involves supplementation of the missing nutrient, either orally or through injection (Mayo Clinic staff, 2011l)Hemolytic AnemiaLack of red blood cells in the blood due to early destruction of the cells....

This paper "Sickle Cell Anemia: Types, Symptoms" discusses developing a cure for the disease.... hellip;  Sickle Cell Anemia (SCA) or drepanocytosis is a common form of sickle cell disease, a fatal disorder which distorts the normal biconcave shape of the red blood cells to a rigid, sickle (crescent) shape.... The therapy remains by far the most successful ever attempted to cure sickle-cell anemia.... The cell sickling occurs as a result of the genetic mutation that results in the formation of abnormal hemoglobin known as hemoglobin S....

For the… ife she has lived, her days of no pain are very countable, and my one greatest fear is that she may never make it to the age of 40 because of the long term effects and prognosis of the disease. Sickle Cell Anemia is a non treatable hereditary problem which has an effect on the Sickle Cell Anemia of the of the Sickle Cell Anemia Introduction I chose to research on Sickle Cell Anemia because my sister has the disease....

The severe episodes of pain in the body are… The disease causes an acute shortage of red blood cells in the body leading to development of an anemic condition Interesting phenomena observed between malaria and Sickle Cell Anemia is that In other words, there are some natural selection traits that favor sickle cell-anemia allele in some individuals.... As such, people from an African descent have the Sickle Cell Anemia allele considering that heterozygotes for the allele are protected from malaria while not showing any significant characteristics of sickle-cell anemia....

The most common form of this disease is Sickle Cell Anemia.... The bone marrow of individuals suffering from Sickle Cell Anemia cannot produce red blood cells fast enough to meet the bodys demand.... Sickle Cell Anemia is an inherited Those with a single inherited gene do not suffer from the disease but possess the sickle cell trait that can be transferred to their children.... As per the National Institutes of Health (NIH) estimates, around 72,000 Americans, most of which are African Americans, suffer from Sickle Cell Anemia (Peterson, 2008)....

Sickle Cell Anemia is characterized by the growth of abnormal hemoglobin, anomalous red blood cells and consequential complications (Olowoyeye & Okwundu, 2010).... This paper is a reflective essay and discusses leadership management on the caring of a patient with sickle cell disorder by applying the theoretical concept from Gibbs framework of reflection.... The essay is based on the case study of a 25-year old African-Caribbean man who had been diagnosed episode of sickle cell pain....

It has been found that people infected by malaria parasites over a long period of time tend to develop this disease of Sickle Cell Anemia completely genetically.... Initially, this disease was referred to as 'Sickle Cell Anemia' but in recent times the word disease has replaced the word anemia.... It has been found that this disease is very well equipped in resisting malaria or in other words Sickle Cell Anemia is a fairly effective resistant against malaria....

 … Sickle Cell Anemia is a genetic disease characterized by a mutation in hemoglobin, resulting in hemoglobin polymerization and resultant cell deformation, especially when there is a deficiency of or low oxygen conditions.... Distortion of these cells increases the risk of infections in Sickle Cell Anemia patients.... A person who is heterozygous for the hemoglobin gene will have fewer sickle-shaped red blood cells and a mild case of Sickle Cell Anemia while a homozygous person for sickle cell is likely to experience a high number of sickle cells and a full-blown case of the disease (Kawthalkar, 2012)....