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
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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 prevalent
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paper‚ the reader will learn about Sickle Cell Anemia. The reader will learn what Sickle Cell Anemia is. The diagnosis of Sickle Cell Anemia will be discussed‚ along with the signs‚ symptoms and treatment for Sickle Cell Anemia. Sickle Cell Anemia is a genetic disorder dealing with the red blood cells within the body. The abnormality deals with the formation of hemoglobin within the blood cells. The hemoglobin abnormality is called hemoglobin S. The Sickle Cell gene need to be inhered from both of
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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 project
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Sickle-Cell Disease Greatly affecting the body’s oxygen levels due to mutated red blood cells‚ sickle-cell disease‚ influences an individual’s childhood in multiple ways: cognitive‚ social‚ emotional‚ and physical development. Sickle-cell disease (SCD) refers to an inherited disorder where abnormal hemoglobin is present in one’s red blood cells. Hemoglobin is the protein in red blood cells responsible for carrying oxygen throughout the body. The deformed sickle hemoglobin in people with SCD can form
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Sickle-cell disease‚ also known as sickle-cell anaemia‚ is a hereditary blood disorder‚ caused by an abnormality in the oxygen-carrying protein hemoglobin found in red blood cells. This leads to a propensity for the cells to assume an abnormal‚ rigid‚ sickle-like shape under certain circumstances. Sickle-cell disease is associated with a number of acute and chronic health problems‚ such as severe infections‚ attacks of severe pain‚ stroke‚ and an increased risk of death. Sickle-cell disease occurs
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Abstract Transitional age youth between the ages of 15-18 who are battling chronic illnesses such as Sickle Cell Disease (SCD) traditionally have a hard time coping to their life style. This causes some to fall into depression and the outlook of the quality of life is decreased also. The eight week study will include six African- American boys and girls from an outpatient clinic that specializes in the medical care of persons with SCD. Participants will meet twice a week for an hour. The Children’s
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Sickle Cell Anemia is an inherited disorder that affects the building of hemoglobin in the body. Hemoglobin is a protein in red blood cells that moves oxygen through the body. People are born with sickle cell anemia when they inherit two abnormal genes from both parents (one from each). People with sickle cell disease has a hemoglobin called hemoglobin S. Normally cells move through the body easily but for people who have sickle cell anemia‚ their cells tend to block blood vessels. Normal red blood
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Summary- This article is about an alternative way to treat Sickle Cell Anemia. Sickle Cell Anemia is caused by an inherited genetic mutation. The mutation prohibits oxygen from being transported to tissues. Typically‚ hemoglobin is made up of two alpha-globins and two beta-globins‚ which can each take or remove a molecule of oxygen. If a copy of the mutation is given by both parents‚ only defective beta-globins will be produced. These beta-globins will latch onto each other instead of to oxygen
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Introduction: What are stem cells? Stem cells are unspecialized cells with the capacity to divide and form specialized cells‚ when the circumstances call for it. There are two sources for stem cells: adult and embryonic. Adult stem cells are multipotent cells‚ which can be found in adult tissues. The cells are thought to reside in “niches” in organs and tissues‚ some of which are bone marrow‚ peripheral blood‚ skeletal muscle‚ brain‚ heart‚ and liver. These cells are capable of dividing following
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