Sickle-cell disease Essays & Research Papers

Best Sickle-cell disease Essays

  • The Discussion on Sickle Cell Disease
    Sickle Cell Disease is an illness that affects people all across the globe. This paper will give a description of the sickness through the discussion of the causes, symptoms, and possible cures. Sickle Cell Disease (SCD) is a "group of inherited red blood cell disorders."(1) These disorders can have various afflictions, such as pain, damage and a low blood count--Sickle Cell Anemia. The overall incidence of SCD is eight out of 100,000 people. However, it is much more widespread in some people....
    1,430 Words | 4 Pages
  • Sickle Cell Disease - 1048 Words
    TREATMENT OPTIONS There is NO cure for sickle cell disease, although new stem cell research is promising. Bone marrow transplant is a potential cure, however finding a matched sibling donor is difficult. Therefore treatment is primarily focused on management of symptoms and prevention of pain episodes. Hydroxyurea (a chemotherapeutic medication) is the only recognized treatment option for the prevention of vaso-occlusive crisis in SCD. It is a prescribed drug for adult patients...
    1,048 Words | 4 Pages
  • Sickle Cell Disease - 995 Words
    Sickle Cell Disease Introduction Sickle cell disease (or sickle cell anemia, as it’s often called) is a disorder of the blood in which red blood cells are misshapen and can resemble a crescent or a “sickle” shape. This can cause numerous health complications. One must inherit the gene from both parents for it to become active, due to the fact that it is recessive. Patients with sickle cell disease have a mutation in a gene on chromosome 11 that codes for the beta subunit of the hemoglobin...
    995 Words | 3 Pages
  • Sickle Cell Disease - 615 Words
    Sickle Cell Disease Physical-Adult • Eye problems. The retina, the "film" at the back of the eye that receives and processes visual images, can deteriorate when it does not get enough nourishment from circulating red blood cells. Damage to the retina can be serious enough to cause blindness. • Jaundice, or yellowing of the skin, eyes, and mouth. Yellowing of skin and eyes. These are signs of jaundice, resulting from rapid breakdown of red blood cells. • Delayed growth and puberty in...
    615 Words | 2 Pages
  • All Sickle-cell disease Essays

  • Sickle Cell Disease - 1110 Words
    Thao Tran Prof.Thomas Hematology 09/08/2012 Sickle Cell Disease Blood has been considered the essence of life for centuries, and our blood is a living tissue made up of liquid and solids. There are many diseases related to blood such as anemia which is the decrease in oxygen supply to tissue and causes hypoxia, thalassemia is the mutation in one or more globin gene of hemoglobin, etc. Therefore, one of blood disorders is the most common symptomatic hemoglobinopathy with the greatest...
    1,110 Words | 3 Pages
  • Sickle Cell Disease - 1039 Words
    Sickle-Cell Anemia is a genetic blood disorder caused by the presence of an abnormal form of hemoglobin. These hemoglobin molecules tend to aggregate after unloading oxygen forming long, rod-like structures that force the red cells to assume a sickle shape. Unlike normal red cells, which are usually smooth and malleable, the sickle red cells cannot squeeze through small blood vessels. When the sickle cells block small blood vessels, the organs are deprived of blood and oxygen. This leads to...
    1,039 Words | 3 Pages
  • sickle cell disease - 507 Words
    ‘How could natural selection increase the number of children born with sickle-cell disease in certain regions when these individuals are unlikely to survive and produce offspring?’ Darwin’s theory proposes that 3 conditions are a requisite for natural selection to occur. They are a struggle for existence of the offspring as they are competing for limited resources, variation within species which gives some individuals advantage over others hence better chance of survival and lastly...
    507 Words | 2 Pages
  • Sickle Cell Disease & International Relations
     SC disease, an autoimmune recessive condition, is an inherited abnormality of red blood cells. Affected children inherit two copies of an abnormal hemoglobin gene, one from each parent. For couples where both individuals carry one copy of the abnormal gene, described as having SC trait or being a carrier for SC disease, there is a 1 in 4 chance of future children being affected by the disease (?) From a biomedical perspective, a high potential for benefit from sharing research-generated SC...
    2,090 Words | 6 Pages
  • Evolution of Disease Sickle Cell Anemia
    Evolution of Disease Sickle Cell Anemia Sickle Cell Anemia is a disease that which the red blood cells form an abnormal sickle or crescents shape. Red blood cells are very important to the human body because they carry oxygen throughout the body. The main causes of Sickle cell is when the cells in the body mutate into abnormal cell called haemoglobin S. Haemoglobin S causes the red blood cells to become sickle shaped, rigid. This causes to make it more difficult for the cells to flow the...
    800 Words | 2 Pages
  • Case Study Sickle Cell Disease
    Case Study 97 1. Sickle cell disease is a group of disorders that affects hemoglobin, the molecule in red blood cells that delivers oxygen to cells throughout the body. People with this disorder have atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape. SCD affects millions of people worldwide, particularly those with African, Spanish, Mediterranean, and Indian ancestry. Some 120,000 infants are born with SCD every year...
    798 Words | 3 Pages
  • sickle cell - 439 Words
    Sickle Cell Disease is both a debilating condition and possibly an evolutionary fix. This paper will describe what sickle cell disease is, who carries sickle cell disease, how it is passed on, its symptoms, how it came about and current and future cures for it. What is Sickle Cell Disease? Sickle Cell disease is made up of a collection of red blood cell disorders. Sickle Cell disease is hereditary meaning it is only passed down through the family on a genetic level and cannot be contracted...
    439 Words | 2 Pages
  • Sickle Cell - 345 Words
     Hello Mr. and Mrs. Jones. I would like to let you know that if you do have a baby, you are risking him or her having Sickle Cell Disease. What this is is it’s a disease that is genetically inherited and it involves the red blood cells. Mutations in the HBB gene cause this disease. This disease is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell will have mutations. The parents of offspring with an autosomal recessive gene each carry one copy...
    345 Words | 1 Page
  • Sickle Cell - 479 Words
    Takiya Clausell Our Different Cell’s July 18, 2011 Sickle cell anemia is an inherited blood disease that means you are born with it and it lasts a lifetime. People with sickle cell anemia inherit two variant or sickle cell genes, one from each parent. In the United States, sickle cell anemia affects about 72,000 people. About 2 million Americans carry the sickle cell trait but about 1 in 12 African Americans have the trait. The signs and symptoms of sickle cell anemia...
    479 Words | 2 Pages
  • Sickle Cell - 2570 Words
    SCD also known as sickle cell disease affects the blood and cardiovascular system. There are six different types of SCD. The following discussion will include cause, symptoms, diagnosis, treatment and prevention. The proper education on this disease will give patients and the public a better knowledge of the common unfamiliarity with SCD. The cardiovascular system consists of the heart, arteries, capillaries, veins, and blood. The organs in the cardiovascular system are a vital part of the...
    2,570 Words | 6 Pages
  • Sickle Cell - 1572 Words
    Sickle Cell Anemia is a hereditary disease that changes the smallest and most important components of the body. A gene causes the bone marrow in the body to make sickled shapes, when this happens; it causes the red blood cell to die faster. This is what causes Hemolytic Anemia. Older children and adults with sickle cell disease may experience a few complications, or have a pattern of ongoing problems that shorten their lives. The most common and serious complications of sickle cell disease are...
    1,572 Words | 4 Pages
  • Sickle Cell Research Paper
     Sickle Cell Disease 11/17/14 This research informs the reader about Sickle cell disease. The goal is to raise awareness by describing what the disease is and where it originated. It gives advice on how to recognize signs in a crisis and how to help prevent any further symptoms. This focus uses facts from medical websites such as Web MD and Mayo Clinic. This research highlights every thing there is to know about sickle cell disease through detailed descriptions of where it...
    2,159 Words | 5 Pages
  • Sickle Cell Anemia - 568 Words
    SICKLE CELL ANEMIA Dillon Lukacs Normal Circulatory system  In a normal circulatory system blood flows easily through the veins and arteries. Oxygen is delivered throughout the body to all the vital organs. Sickle Cell Disease  An anemia is a condition where there are less red blood cells than normal. Sickle cell anemia is a disorder where the body creates sickle or crescent shaped red blood cells. In a normal blood cell they look like donuts with a hole in the middle. This shape helps...
    568 Words | 4 Pages
  • Sickle Cell Anemia - 1567 Words
    Physiology Of Flight Term Paper DERYL OMATSEYE Everglades University Mr. Kirk Webster Sickle Cell Anemia Sickle cell anemia or also known as sickle cell disease is a hereditary genetic disease defined by the presence of odd shaped crescent-shaped red blood cells instead of the regular round disc like shape cells. Red blood cells transport oxygen from the lungs to various other organs and tissues with the help of a protein called hemoglobin. The main cause of sickle cell disease...
    1,567 Words | 5 Pages
  • Sickle Cell Anemia - 1338 Words
    The sickle cell disease is an inherited blood disorder that affects red blood cells. People with sickle cell have red blood cells that have mostly hemoglobin's, Sometimes these red blood cells become sickle-shaped or crescent shaped and have trouble going through small blood vessels. When sickle-shaped cells block small blood vessels, less blood can get to that part of the body. Tissue that does not get a normal blood flow eventually becomes damaged.This is what causes the problems of...
    1,338 Words | 5 Pages
  • Sickle Cell Paper - 789 Words
    Sickle Cell Disease (Anemia) Child and Adolescent Development (PSC 1246A) Sickle Cell Disease, commonly referred to as Sickle Cell Anemia, is a blood disease which red blood cells form an abnormal sickle or crescent shape. Red blood cells carry oxygen to the body and are normally shaped like a disc. This disease is genetically inherited from both parents. If you inherit the sickle cell gene from only one parent, you will have sickle cell trait. People with sickle cell...
    789 Words | 2 Pages
  • Sickle Cell Anemia - 813 Words
    Sickle Cell Anemia Pathophysiology: Sickle cell anemia is a disease passed down through families in which red blood cells form an abnormal crescent shape. The “sickling” occurs because of a mutation in the hemoglobin gene. Sickle cells are stiff and sticky. They tend to block blood flow in the blood vessels of the limbs and organs. Blocked blood flow can cause pain, serious infections, and organ damage. Life expectancy in people who have this disease is shortened. Anemia is a condition in...
    813 Words | 3 Pages
  • Sickle Cell Report - 667 Words
    What is it? Sickle cell anemia is a type of blood disorder that can be inherited from parents. This is when red blood cells that are meant to carry oxygen around the body become deformed. Normal red blood cells are round and disc shaped, however, when they become sickle red blood cells, the deform and change shape into a crescent-like shape or sickle shape. The sickle cells have a shorter life-span than a healthy red blood cell and are not replaced as quickly as normal; this leads to a...
    667 Words | 3 Pages
  • Sickle Cell Anemia - 1001 Words
    Sickle Cell Disease: Journal Article Review Kelsey Bowman Bio 204: Anatomy and Physiology 2 Zellers Sickle cell disease is an autosomal recessive genetic disorder most common in African Americans, which results from a mutation affecting the amino acid sequence of the beta chains of hemoglobin molecules in red blood cells. The abnormal hemoglobin which causes the red blood cells to sickle is called hemoglobin S. Sickling occurs when the red blood cells are deoxygenated...
    1,001 Words | 3 Pages
  • Sickle Cell Anemia - 689 Words
    Anemia is a condition in which there is lower than normal number of red blood cells or hemoglobin within a person, consequently decreasing the amount of oxygen being carried to the rest of the body. Causes of such a condition are usually insufficient amounts of iron, blood loss, lack of red blood cell production, or high rates of red blood cell destruction. (MNT, One form of this condition is the disease Sickle Cell Anemia, an inherited blood...
    689 Words | 2 Pages
  • Sickle Cell Anemia - 5318 Words
    Sickle Cell Anemia Jenkins 1 Abstract Sickle Cell Anemia is a hereditary disease that changes the smallest and most important components of the body. A gene causes the bone marrow in the body to make sickled shapes, when this happens; it causes the red blood cell to die faster. This is what causes Hemolytic Anemia. Older children and adults with sickle cell disease may experience a few complications, or have a pattern of ongoing problems that shorten their lives. The most...
    5,318 Words | 16 Pages
  • Sickle Cell Anaemia - 531 Words
    SICKLE CELL ANAEMIA Sickle cell anemia is an inherited condition. People with sickle cell anemia inherit two copies of the sickle cell gene, one from each parent. The sickle cell gene makes abnormal hemoglobin called Hemoglobin-S. The sickle cell gene is a trait due to a change in ONE nucleotide in the DNA sequence that leads to a change in ONE amino acid that changes how the hemoglobin protein folds. This change in the structure of the hemoglobin protein leads to a change in the shape...
    531 Words | 2 Pages
  • Sickle cell anemia - 1235 Words
    Sickle cell anemia (SCA) also known as sickle-cell disease (SDA) is the most common genetic blood disorder that most people know far to little about. It is blood disease identified by abnormal looking red blood cells (Primary Health Care 2012). Normal blood cells tend to be soft and round and travel to through the body smoothly as for sickle cells, on the other hand, look like a hard falcate moon shape (Primary Health Care 2012). These abnormal red blood cells result in a difficult blood flow...
    1,235 Words | 4 Pages
  • Sickle Cell Anemia - 1832 Words
    Sickle Cell Anemia Sickle Cell Anemia occurs in about 1 out of 500 African American births, and 1 out of 36,000 Hispanic births. It is a lifelong disease, and sometime can be deadly. According to Dr. Whittaker, in our region there are abnormally higher cases of Sickle Cell Anemia, so I found it important to learn more about the disease, what cause it, what are the symptoms as well as the options of treatments for this disease. According to, it is believed that sickle cell...
    1,832 Words | 5 Pages
  • Sickle Cell Anemia - 782 Words
     Sickle cell anemia is a disease that changes normal round red blood cells into cells that are shaped like crescent moons. Sickle cell comes from a farm tool with a curved blade. Sickle cells get stuck and block blood vessels which stop the oxygen from getting through. This causes a lot of pain and can also harm organs, muscles, and bones. Sickle cell is a lifelong battle that causes pain, infection, anemia, and even a stroke. Sickle cell is an inherited disease. It used to be that when people...
    782 Words | 2 Pages
  • Sickle Cell Paper - 1457 Words
    Sickle Cell Imagine an illness at birth that causes lifelong complications for the child, the family, and the healthcare providers. Sickle-cell is a disease that affects thousands of people around the world and unfortunately that number continues to grow. Sickle-cell is a disease that many healthcare workers will encounter, especially in the acute care setting. It is important that nurses can recognize the symptoms and know how to treat these patients. With proper treatment and care, many...
    1,457 Words | 5 Pages
  • sickle cell anaemia - 1640 Words
    Introduction - sickle cell anemia The first suggestion that genes might provide the information for all proteins came from Linus Pauling's lab at Caltech. He and his student Harvey Itano studied hemoglobin, the protein in red blood cells that transports oxygen from the lung to metabolically active tissues, like muscle, where it is needed. In particular, they focused on the hemoglobin of people with sickle-cell disease, also known as sickle-cell anemia, a genetic disorder common in Africans,...
    1,640 Words | 5 Pages
  • Sickle Cell Anemia - 1345 Words
    Sickle Cell Anemia Sickle cell anemia is an inherited blood disease. The word anemia is defined as meaning that the blood does not have the required number of red blood cells. These cells take on a crescent shape, which is where the disease takes its name from the abnormal sickle shapes of the cells. It is commonly found in people from Africa, the Mediterranean region, southern India and the Middle East. “This disease of the blood was first discovered in 1910 in a black college student from the...
    1,345 Words | 4 Pages
  • Genetics of Sickle Cell Anemia
    Genetics of Sickle Cell Anemia Objectives • To observe how a disease can act as a selective force • To describe changes in allele frequencies in a population as a result of a selective force Hypothesis The starting ratio of HbA to HbS is 3:1; in a typical population, the Homozygous Dominant Gene would become the standard, but because carrying the Heterozygous version of the allele has an advantage to fighting Malaria it will become the dominant Allele for the population. The HbA/HbS gene...
    774 Words | 3 Pages
  • Sickle Cell PP - 457 Words
    SICKLE CELL ANEMIA Tina Thompson, Ashley Scott, Araceli Galindo, Roshanda Dixon, Kristen Wyatt, Kimberly Dennis What is Sickle Cell Anemia?  Sickle cell anemia is a severe hemolytic anemia resulting in a sickle shaped hemoglobin molecule. It is an inherited disorder with some having sickle cell trait and some having sickle cell disease. The sickle hemoglobin gene is known as the HbS gene. It is found predominantly in people of African descent and occasionally in those of Mediterranean...
    457 Words | 5 Pages
  • Sickle Cell Anemia - 621 Words
    Sickle Cell Anemia Sickle cell anemia is an inherited blood disorder, identified by the sickle shape of red blood cells which carry less oxygen and break easily, causing anemia. The sickling trait, the less serious form, occurs from the inheritance of only one parent; however, both parents must exhibit the disease in order for full symptoms to take place. It is caused by an error in the gene that tells the body how to make hemoglobin. The disorder is usually found in people of African...
    621 Words | 2 Pages
  • Sickle Cell Plan of Care
    Sickle Cell Plan of Care Read the situation provided. Then, provide a brief description of the pathophysiology of sickle cell anemia and complete the nursing care plan by filling in the goals, outcomes, and nursing orders for the diagnoses provided in the table. SITUATION: Lavon is a 30 year old, single African American who was diagnosed with sickle cell anemia when he was 4 years old. He works for a computer company and has been working 12 hour days to meet the deadline for a special...
    610 Words | 2 Pages
  • Sickle Cell Anemia - 847 Words
    The erythrocytes of certain individuals possess the capacity to undergo reversible changes in shape in response to changes in the partial pressure of oxygen. When the oxygen pressure is lowered, these cells change their forms from the normal biconcave disk to crescent, holly wreath, and other forms. This process is known as sickling. What is Sickle Cell Anemia? It is a blood disorder that affects hemoglobin, red blood cells with normal hemoglobin move easily through the bloodstream,...
    847 Words | 3 Pages
  • Sickle Cell Anemia - 2034 Words
    There have been many researches and tests done on the genetic causes of Sickle Cell Anemia and how it developes, as well as it's effects on the circulatory, muscular, and respiratory systems, as well as it's effects on the joints and other systems of the body, and the complications associated with them. Most of the research has been done to explore on the reasons why it mostly effects the African-American community and people who are from the West Coast of Africa. It has also been known that...
    2,034 Words | 6 Pages
  • Sickle Cell Lab - 1314 Words
    Observations: When Malaria is present and infects red blood cells, parasites can infect cells carrying defective hemoglobin which may result in death. Allele frequency changes over time depending on the pressures or circumstances facing a particular population. African populations are especially impacted by both malaria and sickle cell anemia. Depending on the impacted population, allele frequency often shifts and well suited organisms are likely to survive and allele frequencies can...
    1,314 Words | 4 Pages
  • Sickle Cell Anemia - 518 Words
    Internet Research Paper For Sickle Cell Anemia The definition for sickle cell anemia is an abnormal, rigid, sickle shape. Sickling decreases the cells flexibility and results in a risk of various complications. Sickle cell is the name of a specific disease in which there is a homozygosity for the mutation that causes Hbs. This type of disease, usually presenting in childhood, occurs more commonly in people from parts of the tropical and sub-tropical regions where malaria is more common....
    518 Words | 2 Pages
  • Sickle Cell Anemia - 2191 Words
    Sickle cell anemia Sickle cell anemia is a disease found right here in America, but in low levels compare to most of the world. The rate for disease is around five times greater in certain places in Africa. Sickle-Cell Anemia is often referred to as the “Negro-Inherited” disease, but that is incorrect. Although African Americans have a high occurrence of Sickle-Cell Anemia (1 in 400 African Americans), many other nationalities suffer from the disease. Sickle-Cell Anemia affects 8 out of...
    2,191 Words | 6 Pages
  • Sickle Cell Anemia - 3192 Words
    Sickle cell crisis (HgbSS) is a debilitating disorder characterized by blood cells changing into a sickle shape as a result of stressful conditions such as exhaustion, hypoxia, severe infection, or even cold temperatures. "The term sickle cell disease (SCD) is used in a generic sense to refer to all the clinically severe sickling syndromes" (Desai,Dhanani, 2002). This paper is going to describe the theoretical origin of sickle cell, the genetic components, pathophysiology of the sickle cell...
    3,192 Words | 8 Pages
  • Sickle Cell Anemia - 877 Words
    The problem is that sickle cell anemia affects about 72,000 Americans in the United States. Sickle cell anemia is an inherited disease in which the body is unable to produce normal hemoglobin, an iron-containing protein. Abnormal hemoglobin can morph cells that can become lodged in narrow blood vessels, blocking oxygen from reaching organs and tissues. The effects of sickle cell anemia are bouts of extreme pain, infectious, fever, jaundice, stroke, slow growth, organ, and failure. Sickle...
    877 Words | 3 Pages
  • sickle cell anemia and alcohol
     Sickle cell anemia Name Institution Sickle cell anemia Introduction Sickle cell anemia is a hereditary disorder that affects countries that were previously affected by malaria - mostly the African Americans and Hispanic Americans (Newland, 2013). The people suffering from this disorder have in the past had barriers to access vital health information and care since it was not covered by the affordable act. At the same time, the disorder has had psychological,...
    697 Words | 3 Pages
  • Pain Management and Quality of Life for Sickle Cell Disease Patients
    Pain Management and Quality of Life for Sickle Cell Disease Patients Cynthia Evans Mississippi College Pain Management and Quality of Life for Sickle Cell Disease Patients This is a review of literature examining how frequent recurring episodes of pain affect the quality of life in the sickle cell disease patients. Several studies conducted concerning pain management and quality of life for sickle cell disease patients indicate additional studies needed. Identifying additional...
    1,713 Words | 5 Pages
  • Sickle Cell Anemia - 840 Words
    Sickle cell anemia is a genetic blood disorder which is inherited from both parents, that causes red blood cells in patients to be sickle-shaped. This causes the red blood cells to clump together, and be unable to retain oxygen. Sickle cell anemia was first noted in 1910, and is thought to have evolved as a way for the body to naturally fight malaria. It is most prevalent in Africa, India, the West Indies and the Mediterranean, places where malaria is more common. In this country, it is most...
    840 Words | 3 Pages
  • Sickle Cell Anemia - 622 Words
    Sickle Cell Anemia Sickle Cell Anemia is a blood disorder that shortens the life span of red blood cells, and eventually the organisms they are located in. Sickle Cell Anemia is an inherited blood disorder that changes that structure of red blood cells. In a healthy organism, red blood cells are disk shaped and move easily through the blood vessels. In an organism that has sickle cell anemia the red blood cells’ structures are corrupted; instead of the disk-like shape, the red blood cells...
    622 Words | 2 Pages
  • A Brief Description of Sickle Cell Anemia
    Adams 1 Dwayne Adams Instructor: Croshaw Medical Terminology 1 18, April 2013 Sickle Cell Anemia Sickle-cell Anemia is a genetic blood disorder caused by the presence of an abnormal form of hemoglobin molecules in which the red blood cells loose their disc-shape and become crescent shaped. The shape also known as “hemoglobin S”. unlike normal red cells which are usually smooth and malleable, tend to collect after releasing oxygen, and cannot squeeze through small blood vessels. The...
    1,165 Words | 5 Pages
  • Sickle Cell Anemia Case Study
    Alexandria Agee Ms. Songer AP Biology February 16 2015 Sickle Cell Anemia: Case Study Summary Sickle Cell Anemia is a painful diseases that is caused by a mutation in the protein called hemoglobin which helps carry oxygen in red blood cells. Because of the mutation, the hemoglobin is shaped oddly which results in pain because it is hard for the blood to travel throughout the body and anemia because of the lack of oxygen in the blood. A person can only have this disease if both parents are...
    909 Words | 3 Pages
  • Disease - 1484 Words
    What is Health? • Health is a state of complete physical, mental, and social well-being and not merely the absence of disease or infirmity. What is disease? • An abnormal condition of an organism which interrupts the normal bodily functions that often leads to feeling of pain and weakness, and usually associated with symptoms and signs. Types of Diseases Pathogenic • Caused by parasitic organisms (Pathogens). • Pathogen invades the body by contact with infected person. • It is...
    1,484 Words | 11 Pages
  • Anthropology: Well Suited to Understand Sickle-Cell Anemia
    Anthropology Exam #1 Rachel Gargano Fall 2013 Question #2 why does the holistic approach of anthropology make it well suited for understanding sickle- cell anemia? The definition of holism applied to anthropology helps to get started answering this question. Holism in Anthropology generally means all the different parts of something and how those parts work together. Understanding genetic structure and who we are as humans is important to understanding different genetic mutations...
    1,593 Words | 5 Pages
  • Critical Care Nursing: Sickle Cell Anemia
    Critical Care Nursing: Sickle Cell Anemia Critical Care Nursing 10/15/2009 Sickle cell anemia affects millions of people worldwide. Sickle cell anemia is a disease in which your body produces abnormally shaped red blood cells. They don't last as long as normal, round red blood cells, which leads to anemia. Sickle cells contain abnormal hemoglobin that causes the cells to have a sickle shape. Sickle-shaped cells don’t move easily through your blood vessels....
    2,832 Words | 8 Pages
  • Mutative Diseases - 947 Words
    When a person is born, their DNA is subject to many different mutations throughout their life. Some of which are inherited from their parents, they develop at birth or during their adulthood. Some of these mutations are harmless and can go unnoticed for your whole existence, while others can alter your health drastically. There are some mutations that are considered to be valuable, as well as a silent one which does not affect you at all. The mutations heard about most often are those that...
    947 Words | 3 Pages
  • Communicable Diseases - 723 Words
    Communicable Disease * Keep in mind all have fever, swollen LN, rash etc. Scarlet Fever: * Cause: Group A beta Hemolytic Streptococcus * Spread via direct contact/droplet * May lead to RF * Uvula/pharynx beefy red; tonsils have white exudate, pinpoint lesions on palate * Sandpaper rash * Pastina Sign: hyperpigmentation at joints * TONGUE (white furry white strawberry strawberry ) * So throat culture if they have strept/sore throat *** Anybody with a sore...
    723 Words | 4 Pages
  • Genetic diseases - 1676 Words
    Sickle cell anaemia: Sickle cell anaemia is an inherited genetic blood disorder in which red blood cells, which carry oxygen around the body, develop abnormally. Rather than being round and flexible, the sickle red blood cells become shaped like a crescent. These abnormal red blood cells can then clog sections of blood vessels leading to episodes of pain which can be severe. These episodes are called a sickle cell crisis. They can last from a few minutes to several months, though on average...
    1,676 Words | 5 Pages
  • The two neurological disorders that I will be discussing are Sudden infant death syndrome and sickle cells
     The two neurological disorders that I will be discussing are Sudden infant death syndrome and sickle cells anemia. Sudden death syndrome is a disorder in which healthy infants die in their sleep. This disease has strike over 2,500 infants while napping or sleeping through the night. This pattern only occur through normal breathing during sleep. Although, it has been determine that they neither choke or smoother while sleeping. They just die a peaceful death. It has been suggested that parents...
    497 Words | 2 Pages
  • Research Proposal: What Ate Staff Nurses Perspectives on Physical and Psychological Barriers to Care in the Treatment of Sickle Cell Anemia Patients in Acute Crisis?
    A Research Proposal: What are Staff Nurses Perspectives on Physical and Psychological Barriers to Care in the Treatment of Sickle Cell Anemia Patients in Acute Crisis? Abstract The staff nurse in the inpatient setting is perhaps the provider with the most frequent interaction and care interventions during the acute stay of a client with sickle cell anemia. A review of the current nursing literature prompted the current study to expand inquiry into the physical and psychological barriers...
    4,675 Words | 14 Pages
  • Sickel Cell Anemia - 1300 Words
    Sickle Cell anemia is a group of inherited red blood cell disorders, or a collection of recessive genetic disorders characterized by a hemoglobin variant called Hb S. Normal red blood cells are round like doughnuts, and they move through small blood tubes in the body to deliver oxygen. Sickle red blood cells become hard, sticky and shaped like sickles used to cut wheat. When these hard and pointed red cells go through the small blood tube, they clog the flow and break apart. This can cause pain,...
    1,300 Words | 4 Pages
  • What s sikcle cell?
    What Is Sickle Cell Anemia? Sickle cell anemia (uh-NEE-me-uh) is the most common form of sickle cell disease (SCD). SCD is a serious disorder in which the body makes sickle-shaped red blood cells. “Sickle-shaped” means that the red blood cells are shaped like a crescent. Normal red blood cells are disc-shaped and look like doughnuts without holes in the center. They move easily through your blood vessels. Red blood cells contain an iron-rich protein called hemoglobin (HEE-muh-glow-bin). This...
    2,886 Words | 9 Pages
  • Module Title: Theoretical Concepts of Health and Disease
    MODULE TITLE: Theoretical Concepts of Health and Disease Marcia Hylton Introduction Sickle cell disease is an umbrella term used to describe a group of inherited disorders of the haemoglobin known as haemoglobinopathies and includes Sickle Cell Anaemia, which generally is the most severe form. It is found in people of African and Caribbean origin and to a lesser extent in people of Mediterranean, Asian and Middle Eastern origin. People of these origins live all over the world, therefore the...
    796 Words | 3 Pages
  • nursing process paper - 3297 Words
    B. Parker Prof. Fern Baudo December 4, 2013 Nursing Process Paper ! Managing ineffective health maintenance in a patient with multiple chronic illnesses. Overview. M.E.P. is a 37 year old African-American female who came to the ER on September 20, complaining of widespread severe body pain, shortness of breath, weakness, extreme fatigue, and a fever. In the ER, the physicians admitted her to inpatient care with two diagnoses: sickle cell anemia crisis and mycoplasmic...
    3,297 Words | 10 Pages
  • Disruptions in Homeostasis - 992 Words
    Homeostasis is the maintenance of a constant environment in response to internal and external stimuli. The body requires the constant and healthy environment that only homeostasis can provide Without this environment the body wouldn’t be able to carry out the life support process. An example of a normal disruption in homeostasis would be if one were to raise the temperature. The body would respond by ejecting and liquid from your body, called sweat. Sweating is meant to cool down the body....
    992 Words | 3 Pages
  • Acute Pain - 427 Words
    Nursing Diagnosis: Acute pain related to vasoocclusive crisis hypoxia, which causes cells to become rigid and elongated, thus forming the crescent shape as evidenced by tenderness on palpation and complaint of localized pain. Goal: Be relaxed and comfortable with controlled pain (<2/10) throughout stay until discharge. Interventions | Rationale | Assess knowledge of disease and prescribed management | Patients need to understand that sickle cell anemia is a chronic...
    427 Words | 2 Pages
  • Unit 015 Outcome 1 1 2 3 4 The responsibility of the paediatric first aider
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