Sickle Cell Anemia INTRODUCTION “Sickle cell anemia is a disease passed down through families in which red blood cells form an abnormal crescent shape. It is caused by an abnormal type of hemoglobin called hemoglobin S” (Sickle cell anemia, 2011). Hemoglobin is an iron-rich protein and an important component of blood…
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This paper briefly analyses various characteristics of Sickle cell anemia. DESCRIPTIVE STATISTICS Anemia is a condition in which the number of red cells in blood decreases beyond certain limits. It can occur because of lack of hemoglobin and defective functioning of hemoglobin. Sickle cells contain sickle hemoglobin or hemoglobin S which is causing Sickle cell anemia. The changes in the shape of red blood cells are referred as sickling in medical terms. Sickle shaped means the shaping of red blood cells in the form of a crescent. Normally blood cells are disc shaped and therefore it can move quickly through the blood. However, when it attains the shape of a crescent, mobility of these cells would be decreased. (Kids health: Sickle Cell Anemia, 2011) Sickling can affect the normal functioning of the cells in different ways. It can reduce the flexibility of the cells and thereby various complications can occur to the patient. Life expectancy of the Sickle cell anemia patients has found to be comparatively lower to that of the normal people. Sickle cell anemia is usually appearing at the childhood itself. In areas where malaria is common, Sickle cell anemia found to be more common. In other words, a connection between Sickle cell anemia and malaria cannot be ruled out. ...
It should be noted that normal life span of red blood cells is about 120 days. If red cells die within 10 to 20 days from its production, it is evident that the normal number of red cells cannot be sustained in blood. It is difficult for bone marrow to supply enough red cells based on the demand created by the untimely death of red cells. CLINICAL MANIFESTATIONS If both parents have the sickle cell trait, the chance that a child will have sickle cell disease is 25%. If one parent is carrying the trait and the other actually has disease, the odds increase to 50% that their child will inherit the disease (Sickle cell anemia: patient education, 2011) Sickle cell anemia normally occurs when a child gets two sickle cell genes from his parents. If the child gets the defective gene or hemoglobin from one parent and normal hemoglobin from the other parent, he may develop sickle cell trait. However, such people may not show the symptoms of this disease. Symptoms of Sickle cell anemia may not appear until a child becomes four months old. Unusual pain lasting from hours to days is the major symptom of Sickle cell anemia. In some cases, the pain might be extended for many years. Pain can affect the entire body. “Abdominal pain, Bone pain, Breathlessness, Delayed growth and puberty, Fatigue, Fever, Paleness, Rapid heart rate, Ulcers on the lower legs, jaundice, Chest pain, Excessive thirst, Frequent urination, Painful and prolonged erection, Poor eyesight, Strokes, Skin ulcers” (Sickle cell anemia, 2011) etc are the major symptoms of Sickle cell anemia. DIAGNOSIS CRITERIA “Complete blood count (CBC) test, Hemoglobin electrophoresis, Sickle cell test” (Sickle cell anemia, 2011) etc are some of the
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(“Sickle cell anemia Research Paper Example | Topics and Well Written Essays - 1000 words”, n.d.)
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(Sickle Cell Anemia Research Paper Example | Topics and Well Written Essays - 1000 Words)
“Sickle Cell Anemia Research Paper Example | Topics and Well Written Essays - 1000 Words”, n.d. https://studentshare.org/nursing/1436071-sickle-cell-anemia.
Most pregnant women fear telling their husbands that they should go, be screened, and would rather give birth to children who have sickle cell anaemia. The contributory factor to sickle cell anaemia is the fact that most people lack education about the disease and so are not aware about it.
This paper take a look at some of the various ways that the disease affects the lives of people and how this disease can be controlled and managed without causing death. A series of articles and books have been used here as the main sources for getting the useful information used here.
The article describes the condition of Ryan Clark, safety of Pittsburgh Steelers and the reason why he has been restricted from playing in the upcoming game against the Denver Broncos. The writer has described the limitations a professional player has to face because of sickle cell trait and has also highlighted the underlying pathology of the blood disorder.
The author claims that the dreaded complication of the disease in adults are infarction crises which can manifest as dactylitis, femoral head necrosis, hematuria and stroke. The disease is through autosomal recessive inheritance. Mutation of the HbS gene causes a different type of hemoglobin that causes sickling of red blood cells.
Databases suggest that there are more than 6000 known single gene disorders with an autosomal dominant or recessive or a X-linked inheritance pattern (Human Genome Project Information, 2008). One such single
Around 70,000 people, who are from sub African, even though there are some reports in India, some parts of central and South American areas, southern parts of Europe, and Caribbean regions mostly experience sickle cell anemia. Several children do not show any
The principle was understood to be a decrease in the red blood cells that ultimately caused death of the patient (Gale).
Being the most widespread form of anemia, this is primarily caused due to deficiency of iron in the body-either due to imbalanced diet
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
Research shows that one in 12 African Americans and about one in 100 Hispanic Americans convey the sickle cell attribute, which implies they are bearers of the infection. Sickle cell sickness is brought about by a change in the hemoglobin-Beta gene found on chromosome 11.
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