Aplastic Anemia Research Paper

Sickle Cell Anemia is an inherited form of anemia, a condition in which there isn’t enough healthy red blood cells to carry sufficient oxygen throughout your body. Normally a person has flexible and round blood cells. With Sickle Cell anemia, Hemoglobin molecules in red blood cells, that carry oxygen in the body, are defective causing some of the red blood cells to change and form a sickle, or crescent moon shape.

Anemia is a condition where the number and quality of erythrocytes in the blood decreases. There are several factors that may prompt anemia: blood loss, complications in erythrocyte production, increased erythrocyte destruction, or a combination of these. There are different types of anemia, and they are distinguished by size, shape, or the erythrocyte’s substance.

Anemia is a disorder of the blood. It occurs when your body does not produce enough erythrocytes or red blood cells (RBCs). Without the erythrocytes oxygen can not be adequately delivered to the tissues and organs throughout the body. This will cause you to become weak and tired. A person may also experience headaches, skin pallor, and faintness. Your body may attempt to compensate for these symptoms by speeding up the heart rate and respiratory rate. This is the body’s attempt to return oxygen levels to normal(Thibodeau and Patton, 2005).

The most prominent cause of Iron Deficiency Anemia is bleeding. Blood loss from the Gastrointestinal Tract is a significant cause of anemia for both men and women. When blood is present in excrement, a gastrointestinal problem exists. Many times, people are unaware of these problems with their waste products. When they begin to feel the symptoms of anemia and undergo tests that determine that they are anemic, it begins the process of discovering more health problems. Anemia can serve as the precursor of certain diseases. There are many instances when it is merely a sign of severe disease such as a peptic ulcer disease, gastritis, hemorrhoids, angiodysplasis of the colon, and colonic adenocarcinoma (http://www.physsportsmed.com/issues/sep_96/browne.htm).

According to the study, the symptoms of anemia include malaise, lethargy, fatigue, swelling belly, pale skin, poor appetite, numerous infections, and crankiness.

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, damage and a low blood count, or anemia. There is a substance in the red cell called hemoglobin that carries oxygen inside the cell. One little change in this substance causes the hemoglobin to form long hard rods in the red cell when it gives

Sickle cell is a blood disease. People with sickle cell anemia have crescent moon shaped blood cells that are hard and sticky. When the Sickle cells move through blood tubes, they can clog blood flow and break apart. This can cause main, damage, and a low blood count. The symptoms of the disease are not life threatening, however are not enjoyable. Sickle cell anemia can cause you to experience dizziness, headaches, and shortness of breath. Your skin may also turn more yellow or pale than it usually is. Sickle cell is an inherited disease. It is an unpreventable disease that you are born with. If you have a sickle cell gene, you do not have sickle cell, however your children have a 25% chance of having sickle cell anemia. This blood disorder can cause pain and discomfort but it is unlikely that your life will be in danger if you have the disease.

But, with severe pain crisis hospital provides morphine or oxycodone to help prevent the pain. Anemia is a very common complication of Sickle Cell Disease. When anemia occurs a person might have; pale skin, yellow skin, white eyes, slow growth, and delayed puberty. This brief paragraph will let a person know the main part about sickle cell. On how it is treated, the symptoms, and how it is cause. So, now when a person you know that has sickle cell you can let them know you learned a little about sickle cell to help their friend. I still think people with sickle cell disease still can have a regualer life all they have to do is watch what they do every time. Also, they will need to make sure that they are well hydrated at all times. Once you are not hydrated having sickle cell can be the worse thing because of the pain and how bad it comes. Sickle cell diesaes doesn’t ruin one person life it just take that one person know what they can do and cant do at all times. There are doctors that help with sickle cell too. These doctors’ helps you maintain your pain crisis and let you know what you can and cannot do at

Low blood counts are a key feature of myelodysplastic syndrome which is the reason for the many symptoms these patients experience. The three types of cytopenia that people with Myelodysplastic Syndrome experience are anemia, neutropenia, and thrombocytopenia which are all low blood cell counts of the three blood cells. Cytopenias can cause anemia, the inability to fight off infections, easy bruising, and spontaneous bleeding. This can be due to the lack of blood cells in the blood stream, but also from dysplasia of the blood cells from the disease. If the cell is deformed, it may not be able to provide the same function as a healthy cell, resulting in the same effect as having cytopenia. Myelodysplastic syndrome is a gradual process and is

Sickle cell anemia is a disease you get from having two sickle hemoglobin within your red blood cells. There’s no other way to develop this disease than by genetics, which only occurs if both of your inherited cells are abnormal. Unfortunately, since sickle cell anemia is an inherited disease, there’s no way to prevent

That results in deprivation of oxygen rich blood to the tissues and organs that use and need it. This is what causes the painful episodes that are associated with the disease. This pain can sometimes be related to damage to vital organs such as the spleen, liver, kidneys, pelvic bones, heart, lungs, and even the brain. Serious complications from certain infected tissues can happen. They cycle of a normal red blood cell is around 120 days, sickled cells differ and can only last for 10-20 days long. The red blood cell supply shortens because the body can’t keep up making them as fast as they are dying, so this results in a condition called, Anemia.

Sickle-cell Anemia is a disorder that is typically inherited from a person's parents. Sickle-cell anemia results in an abnormality in the oxygen-carrying protein haemoglobin (haemoglobin S) that is found in red blood cells. In such a condition the red blood cells contort into a sickle shape. The affected cells die early which results to a shortage of healthy red blood cells and can block blood flow causing pain. The disease s caused by gene mutation through the process of substitution. In the Sickle-cell condition one Amino Acid; glutamic acid is always replaced by another acid valine. This happens in each of the two polypeptide chains of the haemoglobin molecule.This alteration results to a haemoglobin type S that is defective and is genetically

blood disorders, such as hemolytic anemia (the rupture or destruction of red blood cells that lead to a decreased amount of red blood cells in your circulation, which leads to fatigue and weakness)

Anemia is a condition in which the concentration of red blood cells or hemoglobin in the blood is below normal. Hemoglobin is a substance in red blood cells that carries oxygen to the tissues of the body. Anemia results in not enough oxygen reaching these tissues.

Aplastic Anemia (AA) can be idiopathic (~70%), inherited (~15-20%) or acquired due to radiation, tablets, viruses or immune disturbances (~10-15%). Idiopathic and secondary AA is generally immune mediated through autoreactive lymphocytes intermediating damage of hematopoietic stem cells. The clinical course of AA is very different, some patients might have only mild symptoms, needed to be little or no therapy, while others with life-threatening