CDC‚ sickle cell disease is a hereditary disease where the red blood cells have an unusual shape that prevents them from moving easily through the blood vessels and satisfying their metabolic needs causing them to die faster. People with sickle cell disease often experience pain due to the sickle cell blocking the small blood vessels‚ anemia due to the low healthy blood cell count‚ and infections. Although it is impossible to obtain accurate information about everyone that has the sickle cell disease
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Sickle Cell Disease (SCD) is a group of inherited red blood cell disorders. People with Sickle Cell Disease have abnormal hemoglobin‚ called hemoglobin S or sickle hemoglobin‚ in their red blood cells. People with SCD inherit two abnormal hemoglobin genes‚ one from each of their parents. One of these abnormal hemoglobin genes causes the production of hemoglobin S in the body.1 When a person has two hemoglobin S genes‚ Hemoglobin SS‚ this disease is called Sickle Cell Anemia.1 This is the most common
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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.
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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 worldwide
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Defects Sickle Cell Anemia (SCA) Sickle Cell Anemia (SCA) is one of a group of diseases collectively termed hemaglobinopathies‚ in which normal adult hemoglobin is partially or completely replaced by abnormal sickle hemoglobin(HgbS). Sickle Cell Anemia includes all of those hereditary disorder‚ the clinical‚ hematologic‚ and pathologic features of which are related to the presence of HbgS. Also know as SS and homozygous sickle cell disease. The most common form of SCD are: Sickle Cell Anemia
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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 disease
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Anemia is a deadly disease; approximately 50% of people with sickle cell anemia survive to mid-40’s although fewer than 10% live more than 60 years. The devastating thong about anemia is that it can be inherited and with no cure‚ the cases of Anemia are increasing. Even though there is no cure‚ early diagnosis of low blood count can lead to better treatment‚ with better treatment‚ patients can live normal lives. However‚ the key to early diagnosis is learning what anemia is and the causes of this
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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 trait
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Anemia Anemia is usually defined as a decrease in amount of red blood cells (RBCs) or the amount of hemoglobin in the blood. It can also be defined as a lowered ability of the blood to carry oxygen. When anemia comes on slowly the symptoms are often vague and may include: feeling tired‚ weakness‚ shortness of breath or a poor ability to exercise. Anemia that comes on quickly often has greater symptoms which may include: confusion‚ feeling like one is going to pass out‚ and an increased desire to
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Anemia ABSTRACT The purpose of this paper is to briefly describe the initial core diagnostic questioning and core set of diagnostic testing related to the patient presenting with anemia. Subjective information and recommended testing are written with consideration of the scope of practice of the family nurse practitioner. In addition‚ three specific case studies are examined. Anemia Core set of subjective questions The healthcare provider should initially obtain a history of any previous
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