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Sickle Cell Anemia Essay Examples

Sickle cell anemia
These cells often fail to return to a more normal shape when normal oxygen levels are restored which leads to many of the complications experienced as a part of the illness. The anemia aspect of the disease is the result of hemolysis, which is...
Pages: 5 (1250 words) , Essay
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Sickle Cell Anemia
In contrast normal hemoglobin is still soluble even when deoxygenated. These sickled cells are rigid and stick to the walls of the capillaries, slowing or stopping the flow of blood and depriving tissues and organs of oxygen. Oxygen deprivation can cause severe pain. Due to...
Pages: 4 (1000 words) , Term Paper
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Sickle Cell Anemia
The condition varies among different people. Sme patients have to live with chronic hurting while others experience regular fatigue (Bogg & Roberts 2009). Te onset of sickle cell anemia is attributed to two genes of sickle hemoglobin that are inherited from both parents, ech contributing...
Pages: 6 (1500 words) , Research Paper , Psychology
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Molecular Biology of Sickle Cell Anemia
1997 pp.479, 481) The hemoglobin molecule shows cooperative binding kinetics, i.e. when one oxygen molecules has been attached, the binding of the rest of the oxygen molecules becomes easier. The oxygen-dissociation curve is sigmoid. It shows that at low partial pressures of oxygen, the hemoglobin molecule...
Pages: 9 (2250 words) , Term Paper , Biology
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Sickle Cell Anemia - Symptoms and Causes
Over time, the persistence presence of Malaria particularly in central and Western Africa began to form a selective pressure, thereby not only influencing the genetic development individuals resistant to the disease but also enhancing their survivability. On the other hand, the Sickle cell is known...
Pages: 6 (1500 words) , Research Paper , Biology
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Sickle Cell Anemia: The Effects of a Childs Illness on the Family
3. Stressful Effects of the Child’s Condition The socio-ecological theory regarding children with chronic diseases posits that the diseased child is in the center of several concentric rings with the family being the most proximal concentric ring to the child in the community. The effects of the...
Pages: 5 (1250 words) , Essay
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A REFLECTIVE WRITING ON CASE STUDY 1 MANAGING A SICKLE CELL ANEMIA FOR ASSESSMENT 2
This cycle constitutes six steps of which the practitioner is expected to provide answers to various questions each leading to the next step, sressing an adequate event analysis provoking decisive thought. Fesh meanings are developed making the learner come up with an affirmative plan of...
Pages: 13 (3250 words) , Essay , Nursing
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Anthropology essay
The complications of this disorder include blockage of the sickle celled red blood cells which causes a lot of pain and eventually organ damage. Individuals with sickle cell anemia suffer from sickle cell crisis attributed to their hypoxic states. They are not able to withstand...
Pages: 4 (1000 words) , Essay
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Genetics of sickle cell
The sequence of discoveries on clinical and pathological features of sickle cell disease are shown in figure 2. Figure 2: Clinical and pathological discoveries on sickle cell disease in chronological order (Rees, Williams and Gladwin, 2010, p. 2019) Studies and surveys have shown that areas where the...
Pages: 7 (1750 words) , Assignment , Biology
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Select a title of your choice within the area of Biology. This is an opportunity to investigate a topic of interest to you that until now you have not yet studied
DISCUSSION More than 60 years ago a German physician and researcher began trying to comprehend the questions of “”how?’ and “why?” this immunity through disease is accomplished. Researchers determined that inside healthy, normal, red blood cells there are short filaments, called actin, which allows the...
Pages: 4 (1000 words) , Essay , Biology
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Describe the biochemical basis of a disease that is a result of a single gene disorder
The sickle cell anemia is an inherited and lifelong disease; patients inherit two genes for the sickle hemoglobin, one from each parent. However, there are instances when people inherit a sickle cell hemoglobin gene from one parent and a normal gene from the other parent,...
Pages: 8 (2000 words) , Essay , Biology
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Sickle cell anaemia
It occurs in the beta globin gene (HBB) which is present in the 11th chromosome. The HBB gene is responsible for normal blood production. The point mutation causes the beta hemoglobin molecule to convert the GAG codon into a GUG codon by transcription, i.e. it...
Pages: 4 (1000 words) , Essay , Biology
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The use of gene therapy to treat genetic diseases
The genetic pattern followed in the inheritance of hemophilia is as follows: i. A normal female and a hemophilic male will bear carrier daughters and normal sons. ii. A carrier female and a normal male have a 50% chance of bearing carrier daughters and 50% chance that...
Pages: 4 (1000 words) , Essay , Biology
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A single gene disorder
Those who carry two SS alleles suffer from sickle cell anemia (Human Genome Project Information, 2008; Genetics, 2000; Gene Gateway- Exploring Genes and Genetic Disorders, 2005; Gene Gateway- Exploring Genes and Genetic Disorders, 2003). Inheritance pattern of sickle cell trait/disease When both the parents are carriers of...
Pages: 4 (1000 words) , Research Paper
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Explain, using statistical data, the epidemiology of one infectious and one non-infectious disease that is widespread in their own country
As cited by Mandell, Bnnett, ad Dolin (2010, p67), vrious public education initiatives are in place to curb HIV spread in Africa. Te South African government aims at reducing sexual transmission of HIV by 50% by 2018 through increasing awareness with male-to-male sexual transmission to...
Pages: 4 (1000 words) , Essay
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Sickle cell disease
These cells mutilated shape (and various different variations from the norm) can keep them from going through little veins, making them aggregate and make blockages that deny organs and tissues of oxygenated blood. Since this frequently excruciating procedure known as vaso-impediment can harm tissue and...
Pages: 5 (1250 words) , Research Paper , Nursing
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Premarital screening (testing) for Thalassemia and Sickle Cell Disease (CSD)
The alpha genes are coded by 4 α genes, paired on each chromosome 16. The non-α genes, namely two γ, one δ, and one β gene per chromosome, are on chromosome 11. Other genes of less significance, the embryonic globin genes zeta and epsilon (ε)...
Pages: 18 (4500 words) , Essay
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Specific Disease that Affects a Particular Minority Group
As we refer to the disorder, the term disease applies because it is an inherited abnormality leading to death or severe complications. However, not all hemoglobin defects are detrimental; this is a concept termed as genetic polymorphism (Serjeant and Beryl, 2001). In the United States of...
Pages: 4 (1000 words) , Research Paper , Health Sciences & Medicine
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Medical Genetic
Hence probability of birth sequence with no linkage = =0.0000153 ix) Newton E. Morton’s formulae calculate the LOD score as, =. This indicates that complete linkage is not possible (i.e.) there is exclusion between the trait and the marker. x) Morgan’s map function ( : Where,...
Pages: 4 (1000 words) , Essay , Biology
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Chronic kidney disease and renal anaemia
Pneumonia is a very severe condition that may result to admission of the patient. Hospitalization would help harbor the effects of the illness from reaching levels that would pose a threat to Solas immunity. Bing a patient with various implications that affect immunity, tere is...
Pages: 10 (2500 words) , Essay , Nursing
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Litrature review related health
Stoke is a medical condition in which here exist an abrupt death of the cells of brain brought about by impairing of the flow of blood to the brain resulting to subsequent lack of enough oxygen to the brain cells. The result of lack of...
Pages: 4 (1000 words) , Essay
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Sickle Cell and it's effects on African Americans in America
An individual with a mild SCD seldom experiences any complications from the illness, whereas a person with a severe SCD is normally incapacitated, experiences bouts of life-threatening complications, and has a smaller chance of surviving into adulthood. Individuals with a mild SCD have the sickle...
Pages: 10 (2500 words) , Essay
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Methods of evaluations for Premarital programs of Thalassemia and SCD
Forty percent prevalence is seen in some regions of Africa (Schwarting, 2007). Infact, Hemoglobin S is most common in persons of African ancestry. In the United States of America, ten percent of the population is at risk of sickle-cell anemia (WHO Secretariat Report, 2006). 10%...
Pages: 10 (2500 words) , Essay
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Human biology
On attaching to the nonciliated epithelia of the fallopian tube in women, mcrovilli surround and move them to the surface having the mucosal cells. Te microbe then uses the process of parasite-directed endocytosia to enter into the epithelial group of cells. I that process, te...
Pages: 13 (3250 words) , Assignment , Biology
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Acute chest sydrome
Thus, radiography also displays certain shortcomings. However, a serial radiography is often helpful in aiding the diagnostic procedure. The method of chest radiography has proven to progress with time though its is a useful form of clinical assessment used in order to identify ACS. Chest...
Pages: 5 (1250 words) , Essay
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Bio-Psycho-Social Assessment
Her sister is excellent academically and very popular which contributes immensely to her relationship with her. Her relationship with her brother is favorable. He is among her favorite among the family. Health and medical issues Apart from her childhood sickle cell anemia disease, she is a healthy...
Pages: 5 (1250 words) , Essay , Sociology
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Essay: Evolution and origins of disease. Darwinian Medicine
The physiological mechanisms associated with the unpleasant experiences will make the body develop its own self-defense (Nesse & George 42). The evolve defenses that causes pain and therefore steers one away from activities that are dangerous to the body. Conflicts with other organisms are also...
Pages: 6 (1500 words) , Essay , Anthropology
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Family Health Assessment
According to Edelman et al., (2010), family values and perceptions touch on the belief systems that govern an individual’s well-being. This Japanese family is strongly rooted in Christianity, a religious belief that has governed their way of life. Unfortunately, their youngest son is suffering from...
Pages: 4 (1000 words) , Essay , Health Sciences & Medicine
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Family Health Assessment
The social group lent them a helping hand during this time. The Family Structure and Function The structure and function of the family was assessed through the use of interviews. It was during this assessment that the effective communication skills of the members of the family came...
Pages: 4 (1000 words) , Assignment , Nursing
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Data Mining In Healthcare
Sets of data which can be effectively converted to useful knowledge that in turn boosts the development of the disease-modifying drugs and curative strategies and therapies. I doing so, te aforementioned practices could also save on medical expenditure, rduce morbidity among SCA patients, ad improve...
Pages: 10 (2500 words) , Research Paper , Information Technology
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Biomedical scences
3. Most of the hemolytic diseases of the newborn (HDN) are caused by the anti-D antibodies which are formed to the RhD agglutinogen. However routine screening of blood types of at risk pregnant patients have eliminated the risk of Rh incompatibility in them. Normally the...
Pages: 13 (3250 words) , Essay , Health Sciences & Medicine
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Transfusion in the patient with Sickle cell Disease
The life of a red blood cell is about 127 days or 4 months (Shemin and Rittenberg, 1946; Kohgo et al., 2008). The main causes of anaemia are blood loss, production of too few red blood cells by the bone marrow or a rapid destruction...
Pages: 24 (6000 words) , Essay
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Sickle Cell Disease
2. Incidence The incidence of sickle cell disease is predominantly in the regions of the world, where malaria is endemic, with particular emphasis on the continent of Africa. Some of the African people have developed partial resistance to malaria genetically. It is believed that blood oriented diseases...
Pages: 8 (2000 words) , Research Proposal
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Sickle Cell Trait
These risks are associated with each pregnancy. Linus Pauling asserts "I have suggested that the time might come in the future when information about heterozygosity in such serious genes as the sickle cell anemia gene would be tattooed on the forehead of the carriers, so...
Pages: 5 (1250 words) , Research Paper , English
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The different types of protein defects that can be associated with the red blood cell
Other cells found in blood include platelets, which assist in clotting, and white blood cells, which serve as the blood’s sentries against pathogens.” Diseases Normal red blood cells are deformable concave disks. The external environment of the cell, the metabolic activity of the cell, the nature of...
Pages: 10 (2500 words) , Essay
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The Major Differences between the Oxygenated and Deoxygenated States of Hemoglobin
In the oxygenated state, the proximal histidine residues as well as the helix carrying it change their positions because of the attachment of an oxygen molecule to heme. This leads to changes in the alpha-beta heterodimers to form the R (relaxed) state. In deoxygenated haemoglobin,...
Pages: 8 (2000 words) , Coursework , Chemistry
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The Human Genome and How Genetic Variation in the Genome Has a Potential Use in Health Screening
Mandated with protecting public health by supervising and scrutinizing of medical procedures such as blood transfusion, selling and purchasing of over the counter medication among others, The Food Drug Administration (FDA) was formed in 1906 under the Public Health Act by the government of the...
Pages: 6 (1500 words) , Research Paper , Biology
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Hemolytic Anemia in G6PD Patients
These variant enzymes cannot produce enough NADPH in red cells to uphold an adequate concentration of concentrated and reduced glutathione. The nonhemolytic variant enzymes are far less susceptible to the inhibition by NADPH because of their low Michaelis constant for NADP and high inhibition constant...
Pages: 4 (1000 words) , Case Study , Health Sciences & Medicine
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Human genetic disorders can arise as a consequence of mutations in either nuclear or mitochondrial genomes. Using specific examples describe the distinct patterns of inheritance for mitochondrial and various nuclear mutations (autosomal, X-linked etc), an
tRNA genes are represented with the name of the amino acid that they bind. The short 7S DNA strand is produced by repeat synthesis of a short segment of the H strand (see Figure 9.2). COMPARISON OF NUCLEAR AND MITOCHONDRIAL GENOME (T. STRACHAN and A. READ,...
Pages: 8 (2000 words) , Essay , Biology
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Nuances of Medical Malpractice Law
Rodney Comeaux was full of complicated health problems since when he was young. Diagnosed with Sickle Cell Anemia at an early age of six months, Rodney was never in perfect health. Sickle Cell Anemia (or SCA) is a genetic abnormality in the blood which is...
Pages: 8 (2260 words) , Case Study , Law
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Rheumatic Fever
Running Head: Age Factor in drawing the Relationship Between Chronic Sickle Cell and Rheumatic Fever Using the Age Factor in drawing the Relationship Between Chronic Sickle Cell and Rheumatic Fever Institution Date Abstract In recent times researchers have become extremely concerned about a subject that has attracted little attention...
Pages: 7 (1750 words) , Essay
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Acute chest sydrome
While other patients will have multiple episodes due to complications such as vasocclusive crisis, hypoxia, postoperatice atelectasis and bronchospasm due to asthma. While the other causes of ACS remain unknown at present, pulmonary infarction and infection are believed to be one of the causes of...
Pages: 6 (1500 words) , Research Paper , Biology
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Resolving Ethical Dilemmas
Ethics in clinical setting refer to the guidelines that have been put in place to aid the physicians in the identification and resolving of ethical issues that they encounter in their duties. The ethical issues include among others informed consent, confidentiality, patients’ rights and truth-telling....
Pages: 2 (500 words) , Essay , Nursing
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Stem cells
That potential of embryonic stem cell therapy to repair process is the greatest; hwever, ehical concerns forbid deep research in this area because embryonic stem cells can be obtained only by the destruction of embryo. Astin, a you may be aware that the spinal cord...
Pages: 4 (1000 words) , Essay , Biology
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Should parents get DNA testing while pregnant
Peace of mind to a pregnant mother is essential since any added stress can be harmful to her and her baby. DA testing normally has a 99.99% of accuracy. Kowing that the DNA test has a high degree of accuracy ascertains the tested person certainly...
Pages: 4 (1000 words) , Essay
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Compare one type of contraception known as Depo-Provera and the biological mechanisms that it uses to different types of contraception and the mechanisms that t
The drug decreases glucose tolerance and hence must be used with caution in diabetes mellitus. The medication must not be repeated in case of occurrence of migraine, diplopia, sudden loss of vision, papilledema or thromboyic complications (Drug Label, Depo-Provera). Side effects...
Pages: 8 (2000 words) , Essay
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Is there a cure for cancer (Human biology)
Hence, the biggest challenge in front of cancer treatment is identification of causative agent and than targeting it. The complexity of causative agent and mulitifactorial influence has made cancer an incurable disease. 2) Systemic nature of Cancer :...
Pages: 6 (1500 words) , Essay
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Bacterial Meningitis
Mode of spread Bacterial meningitis can be contagious through exchanges of pharyngeal and upper respiratory tract secretions in the form of coughing and kissing (cdc.gov). Bacterial meningitis can occur as epidemics. The most common cause of epidemics is meningococcus (Ramakrishnana...
Pages: 4 (1000 words) , Research Paper
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Genetic disorders
Whenever, a mutation occurs, the instructions for producing proteins are altered and thus the entire function collapses, causing the medical condition for genetic disorder. The gene in turn can be inherited from either one parent or also from both the parents. Though genetic disorders are...
Pages: 4 (1000 words) , Essay , History
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Humans versus Nature-- which selects better for human survival, from a biological point of view
In short, te custom-made kids could be available in a decade or so (Jabr 2013). Te nature has built-in wisdom in managing the evolutionary process since ages that mankind is out to derail in the hope of achieving something better; hwever, i all likelihood may...
Pages: 4 (1000 words) , Essay , Anthropology
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