SYMPTOMS AND CURES The symptoms of sickle
SYMPTOMS AND CURES The symptoms of sickle
Survival is key in The Most Dangerous Game and High Noon. Although our two protagonists, Rainsford and Will Kane, run for the beginning of the fight they quickly change that and become the predators. Both Kane and Rainsford end up winning this fight. In the movie High Noon, Frank Miller is coming back to seek revenge on Will Kane. At the end they finally have a shoot off and last man standing, which would be Kane, wins.…
Sickle cell disease is an inherited disorder that is caused by a mutation in the DNA sequences that codes for the beta chain of the hemoglobin protein. Red blood cells are, normally, flexible and round, but with the sickle cell anemia the red blood cells become sticky, rigid, and crescent shaped. The Hemoglobin protein carries oxygen in the red blood cells throughout the body. With the disease, the blood cell’s shape can cause them to get lodged in the blood vessels resulting in the obstruction of blood flow, especially in the smaller arterial vessels in the body This occurrence not only reduces oxygen content to the area of concern, but can be a very painful experience for the victim. People who inherit this disease have two abnormal hemoglobin…
I am in support of the “Sickle Cell Disease Research, Surveillance, Prevention, and Treatment Act of 2015.” Sickle Cell is a serious blood disorder that causes red blood cells to become misshaped. These abnormally shaped red blood cells can get clustered into blood vessels and block blood flow to areas of the body. According to the center of disease and control the number of people with sickle cell in the united states is unknown, but it is prevalent amongst African-Americans occurring in 1 out of 365 births.…
Sickle cell is a disease that affects the circulatory system. The circulatory system is in charge of moving nutrients throughout the entire body with the use of the blood stream. According to hopkinsmedicine.org the circulatory system moves nutrients, water, and oxygen to the your billions of body cells and carries away wastes like; carbon dioxide that body cells create. The circulatory system includes; the heart: which keeps the circulatory system working at all times with its constant pumping; the arteries: which carry oxygen-rich blood away from the heart to where it is needed; veins: they carry oxygen-less blood to the lungs where they have their oxygen then replenished; and lastly the blood,it is like the liquid train of the circulatory…
Renal complications Renal damage is almost inevitable in sickle-cell disease. There is a strong tendency for HbS to polymerise in the renal medulla, because of the low partial pressure of oxygen, the low pH, and the high osmolality causing erythrocyte dehydration. The consequent vaso-occlusion causes renal infarction with papillary necrosis, and medullary fibrosis with focal segmental glomerulosclerosis. Other complications include haematuria, renal medullary carcinoma, nocturnal enuresis (bedwetting), and chronic tubulointerstitial nephritis may occur. Neurological complications Complications occur in 25% of patients, Sickle-cell anaemia is one of the most common causes of stroke in children.…
Sickle cell disease is a major health burden in the Indian community. It contributes to millions of deaths worldwide however it is most prevalent in tribal populations in the rural sectors of India. “Sickle cell disease or SCD is an inherited abnormality of the red blood cell characterized by chronic haemolytic anemia with numerous clinical consequences” (Ugwu 87). The shape of hemoglobin, which gives red blood cells their color is turned from an oval to a crescent shape when the sickle cell gene is present. The sickle shaped cells cause blockage of capillaries which leads to many symptoms such as chronic pain, pneumonia, severe anemia, and increased risk for infections (Powars 1).…
"Sickle cell disease. " The Gale Encyclopedia of Medicine, edited by Jacqueline L. Longe, 5th ed., Gale, 2015. Science in Context, ic.galegroup.com/ic/scic/ReferenceDetailsPage/ReferenceDetailsWindow?disableHighlighting=&displayGroupName=Reference&currPage=&dviSelectedPage=&scanId=&query=&prodId=SCIC&search_within_results=&p=SCIC&mode=view&catId=&limiter=&display-query=&displayGroups=&contentModules=&action=e&sortBy=&documentId=GALE%7CSUKWRU366338883&windowstate=normal&activityType=&failOverType=&commentary=&source=Bookmark&u=pioneer&jsid=22a76abd6c383276c027ddd9c255f1d1. Accessed 21 Nov. 2016.…
In 1910 Sickle Cell Anemia was first discovered and studied by Dr. James B. Herrick. A cardiologist, who was intrigued by the crescent shaped red blood cells. Sickle Cell Anemia is an autosomal recessive genetic disease that is inherited at birth, due to the present of two abnormal hemoglobin gene “S”, one from each parent. Sickle cell anemia is when the red blood cells takes the shape of a sickle; a crescent shaped farm tool used for harvesting or reaping crops. Sickle cell anemia is caused by a mutation on the hemoglobin-beta gene found on chromosome eleven.…
Pain crisis is the primary symptom of SCD; it is caused by sticky, sickle cells forming blood clots resulting in ischemia. Acute chest syndrome is a potentially life-threatening complication that occurs when blood clots collect in the small blood vessels that supply the lungs. Symptoms include fever, chest pain, dyspnea, chills, and hemoptysis. Pulmonary infiltrates are common as well as pulmonary hypertension, and the majority of patients are hypoxemic (Paul, Castro, Aggarwal, & Oneal, 2011). Splenic sequestration is another common complication; rising when the sickle cells become clogged and are trapped in the spleen causing rapid splenomegaly and pain (National Heart, Lung and Blood Institute, 2015).…
This is a disease that gets worse with time, treatments only help lessen complications or prevent them. Treatment options for people vary depending on how bad their condition is. A stem cell transplant would essentially cure a person with the disease, most people do not meet the qualifications for a transplant and even at that, the procedure is still very risky. Usually the first symptom people with Sickle Cell experience, one of the least severe, is swelling in their feet and hands, caused by blockage in the blood vessels. To treat the swelling, pain medicine is usually prescribed and a doctor will recommend an increase in fluids, drink more water.…
Introduction Sickle cell disease is a genetic disorder that can be best described as irregular shaped red blood cells that block blood flow, which cause chronic periodic episodes of pain. Sickle Cells affects over 72,000 Americans and millions throughout the world, Sickle cell most commonly affect African American descent, approximately 1 in 12 African Americans carry the trait for Sickle cell and 1 of every 350 African-American infants born have the disorder and the incidence of the disorder in Africa is ten times higher (AAFP,2000). This paper will highlight background information, causes, diagnosis and discuss several treatment and therapies of Sickle cell disease and why African American are largely affected by this disease. Background…
Sickle cell crisis is an acute condition of sickle cell anemia. Sickle cell anemia is a genetic condition. Both parents must be carriers of the gene in order for a baby to be born with sickle cell anemia. In the United States, the gene predominantly affects black people of African decent. Sickle cell anemia is a disease where there is an inadequate number of healthy red blood cell throughout the body.…
Sickle Cell Anemia is an inherited blood disorder of the red blood cells, which is passed down through families. Sickle cell anemia primarily affects people with African, Mediterranean, Middle Eastern, and Indian ancestry. About 70,000 children are affected with sickle cell anemia because it directly attacks their gene, it is prevalent in African-American and millions of people carry the gene. There are different types of sickle cell disease, People who inherit two sickle cell genes, one from each parent have a type of sickle cell disease called SS, it’s commonly called sickle cell anemia and is usually the most severe form of the disease. People who inherit a sickle cell gene from one parent and a gene for another type of abnormal hemoglobin, from the other parent have a different type of sickle cell disease and some types of sickle cell disease are very severe and the disease affects each person differently.…
Scientist are continuing to prevail in finding treatments and they have been able to find new experimental treatments that can help reduce the pain of sickle cell anemia. These experimental treatments include gene therapy, nitric oxide, statins, and drugs to help boost fetal hemoglobin blood cell…
The signs and symptoms of SCD can vary greatly from person to person, even within the same family and can change over time. Major features and symptoms of sickle cell anemia may include: painful swelling of the hands and feet, known as dactylitis, anemia, frequent infections, vision problems, and severe occurrences of…