Hemochromatosis Research Paper

276 Words1 Page
bulb-icon

Recommended: Essay on hemochromatosis

Hemochromatosis is a disorder that can be inherited from your parents but can also be obtained due to excessive consumption of alcohol or iron or blood transfusions. Hemochromatosis is a disorder that causes your body to absorb more iron than it needs. It then stores the iron in crucial parts of your body like your heart, liver, pancreas, brain, and joints. If the iron continues to built it would lead to iron overload. Iron overload can be fatal because of excessive iron in your heart and liver. Continuous iron overload could lead to serious heart conditions like heart attack and heart failure, it could also lead to liver problems, diabetes mellitus, and possibly cancer and death. Symptoms like diabetes mellitus can be avoided if Hemochromatosis

Show More
Related

  • Cirrhosis Case Study Paper

    2538 Words  | 6 Pages

    1. Outline the causes, incidence and risk factors of the identified disease and how it can impact on the patient and family (450 words)

    Read More

  • Blood Count Case Study

    2573 Words  | 6 Pages

    A complete blood count was done for this patient upon admission in order to give a baseline to help guide his care. The blood count was also done to show how his hematological system was affected by the trauma that he suffered in the motor vehicle accident he was in. If the patient was hemodynamically unstable, he may have needed blood transfusions to bring his blood counts up. White blood cells could help to tell is the patient has an infection in his surgical wound. The patient also underwent surgery to correct the injury to his spine, causing more blood to be lost in the process. The platelet, hemoglobin, and hematocrit counts could help to show in the future if the patient is suffering from internal bleeding after the surgery he had.

    Read More

  • Understanding the Impact of Sickle Cell Disease

    1276 Words  | 3 Pages

    Sickle cell disease is a group of disorders that affects the blood, specifically, a molecule called hemoglobin in red blood cells (“sickle cell disease”, 2016). Hemoglobin is a molecule that facilitates the delivery of oxygen throughout the body (“sickle cell disease”, 2016). A mutant form of the hemoglobin molecule causes red blood cells to become crescent shaped or “sickled shaped” (Lonergan et. al. 2001). This distorted shape of red blood cells causes rigidity of the blood cells and vaso-occulusion (or the blood vessels to become clogged) (Rees et.al., 2010). This often leads to a low number of red blood cells (anemia), repeated infections and episodes of pain that are periodic (“Sickle cell disease”, 2016). Although sickle cell disease

    Read More

  • Sickle Cell Case Study

    1537 Words  | 4 Pages

    What is Sickle cell disease? Sickle cell affects a disease; that disease is called which affects the hemoglobin when the red blood cells that send oxygen through the body are killed off and weakened. Sickle cells can be found in every 1 and 1000 African Americans, it is affecting about 70,000 to 80,000 Americans in the United States. Sickle cell is a death threatening disease, and the severity of symptoms can vary from person to person (Sickle cell disease (SCD), 2015). Some people have light conditions, but others can have severe conditions, which, mean they could be hospitalized. Characteristics of this disease are caused by a minimum of low blood cells, which is called anemia.

    Read More

  • Thalassemia Essay

    886 Words  | 2 Pages

    Thalassemia is an inherited blood disorder characterized by low amounts of hemoglobin and a low count of erythrocytes in the body. Thalassemia is caused by mutations in the deoxyribonucleic acid of cells, which makes hemoglobin. The mutations are passed from parent to child. The mutations vary depending on the type of Thalassemia inherited. The variation in the mutation occurs from the number of gene mutations, which are inherited, as well as mutation within the hemoglobin molecule. Clinical manifestations are diverse ranging from asymptomatic, to those who are carriers of the thalassemia, which may have mild symptoms, there also people who posses the trait, who may have severe symptoms which lead to death.

    Read More

  • Taking a Look at Dialysis

    945 Words  | 2 Pages

    Kidney dialysis comes at a price. With chronic kidney disease (CKD), there can be problems with iron depletion. Dialysis slowly depletes a patient of iron. On average, about 5-7 mg of iron is lost in each session. Until recently, the main way doctors tried to compensate for this loss was by adding 100 mg of iron into the bloodstream. This treatment comes with risks of oxidative stress and can cause liver damage. A new drug has recently been in the news and seems to help greatly with this problem. The drug is called Triferic. Triferic mimics the way iron is absorbed into the body naturally. The absorption gradually goes to the body’s bone marrow and helps to maintain levels of hemoglobin. Triferic is still in the trial stages with 3 successful trials done so far. It very well may become an integrated treatment for those with CKD. (Glatter, 2013)

    Read More

  • Liver Diseases Resulting from Alcohol

    1426 Words  | 3 Pages

    Liver disease resulting from alcohol affects more than two million Americans and is one of the primary causes of illness and death. The liver frees the body of harmful substances, such as alcohol. While the liver breaks down alcohol, it produces toxins that can be even more dangerous than the alcohol consumed (“Beyond Hangovers: Understanding Alcohol's Impact Your Health” 13). “These by-products damage liver cells, promote inflammation, and weaken the body’s natural defenses. Eventually, these problems can disrupt the body’s metabolism and impair the function of other organs” (“Beyond Hangovers: Understanding Alcohol's Impact Your Health” 13). A condition called steatosis is the result of fat build up in the liver and is the earliest stage of alcoholic liver disease. This condition causes the liver difficulty breaking down alcohol, potentially resulting in alcoholic hepatitis. Fibrosis of the liver, which is also related to heavy drinking, causes scar tissue to build up in the liver. The alcohol alters chemicals that the liver needs to break down this scar tissue, causing liver dysfunctions. If one does not refrain from drinking during the condition of fibrosis, the scar tissue can build up and create another condition, called cirrhosis. Cirrhosis is deterioration of the liver resulting from heavy scarring, causing the liver to not be able to function properly. If cirrhosis becomes severe, a liver transplant may be the only solution (“Beyond Hangovers: Understanding Alcohol's Impact Your Health” 14). It is difficult to calculate when a person would develop cirrhosis, because an alcoholic could never develop the disease, but someone who social drinks could. It is also unknown why cirrhosis is more prevalent in women (...

    Read More

  • Essay On Blood Typing

    697 Words  | 2 Pages

    Have you ever given blood? Have you ever been asked what type of blood you have? There are four different blood types, and it is very important to know which kind you have for medical reasons and for the benefit of others.

    Read More

  • Ms. A Case Study Essay

    798 Words  | 2 Pages

    According to the details given in case study, Ms. A has iron deficiency anemia. Iron deficiency anemia is the most common type of anemia. It is a condition where the blood lacks enough red blood cells (Clark, 2008). When there are a low number of red blood cells, it makes transportation of oxygen to parts of the body very difficult. Iron deficiency is type of anemia due to the lack of iron in the body. Without the proper amount of iron in the body, it cannot produce enough hemoglobin and since hemoglobin is the main carrier of oxygen, low levels of it can lead to tiredness and shortness of breath (Copstead, Banasik, 2010).

    Read More

  • Alpha Thalassemia Essay

    2872 Words  | 6 Pages

    Alpha thalassemia is a blood disorder that reduces the production of hemoglobin, which is the protein in red blood cells responsible for carrying oxygen throughout the body. Those affected experience a shortage of efficient oxygen-carrying red blood cells, causing anemia, and manifesting in the observable signs of: pale skin, weakness, fatigue, or serious complications when coupled with other illnesses. Thalassemia is a blood disorder passed down through families (since it is inherited siblings may share this disease) in which the body makes an abnormal form of hemoglobin, resulting in excessive destruction of red blood cells and diminishing the affected person’s normal, healthy red blood cells. Damage to the body is caused by either a genetic mutation or a deletion of HBA1 and HBA2 genes. Because each person inherits two alpha-globin alleles from each parent, when both parents are missing at least one alpha-globin allele, the child is at risk of having Hb Bart syndrome, HbH disease, or alpha thalassemia depending on the number of missing working alleles. Involving the genes HBA1 and HBA2, alpha-thalassemia is due to impaired production of either 1, 2, 3, or 4 alpha globin chains, leading to an excess of beta globin chains. There are four copies of the gene instructing the body to make alpha globin; the more functioning genes a person has, the more alpha globin is made, whereas the number of non-working genes determines what type of alpha thalassemia a person has since when one or more of the alpha globin genes is not working properly, less alpha globin is made. There exist different types of alpha thalassemia: having three normal alpha genes results in a silent carrier state; two normal alpha genes results in mic...

    Read More

  • Sickle Cell Anemia

    859 Words  | 2 Pages

    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.

    Read More

  • Iron Deficiency Anemia

    3211 Words  | 7 Pages

    Iron is a mineral that is found the in hemoglobin of the Red Blood Cells. It facilitates in the transport of oxygen all over the body. Without this mineral, oxygen cannot be carried to its full capacity. 1 out of 10 women and small children have iron deficiencies. Lacking iron causes lethargy and a weakened immune system. Children who do not have an adequate intake of iron put themselves at risk for intellectual developmental problems. However, an iron deficient person is not necessarily anemic. 7.8 million women are iron deficient, while only 3.3 million women are anemic (http://www.mayohealth.org/mayo/9704/iron_def.htm). When the deficiency becomes so severe that the circulating Red Blood Count and the minerals Ht, Hg, and Hem drop below normal, anemia occurs (See Figure 1). The hormone androgen causes men and women to have different normal values of the hemogram (http://www.medstudents.com.br/hemat/hemat4.htm). Low ferritin (iron storage molecule) and high TIBC (tota...

    Read More

  • The Different Types of Thalassemia and How is Diagnosed

    2446 Words  | 5 Pages

    Thalassemia is basically a name for similar groups of inherited blood diseases that involve missing or abnormal genes regarding the protein in hemoglobin which is the red blood cells that carry oxygen throughout the body. I will discuss the different types of Thalassemia, how Thalassemia is diagnosed, and the treatments available. I will also discuss the complications and side effects of the treatments, the disease’s causes and effects, and how it is more dominant in some parts of the world than others. Thalassemia is a blood disorder which means the body makes fewer healthy red blood cells and less hemoglobin. Hemoglobin is a protein that carries oxygen throughout the body and having less hemoglobin leads to anemia. Alpha globin and beta globin are the proteins that create Hemoglobin. A defect in the gene that helps control production of alpha or beta goblin leads to Thalassemia. Fewer blood cells leads to anemia, which is the common culprit in Thalassemia.

    Read More

  • Thalassemia Essay

    720 Words  | 2 Pages

    Thalassemia is a blood disorder transferred through families. It occurs when the body makes less hemoglobin than needed or an unusual form of hemoglobin. Hemoglobin is the protein in red blood cells that carry oxygen. The disorder makes an excessive amount of destruction of red blood cells. This eventually leads to anemia.

    Read More

  • Blood Grouping Essay

    729 Words  | 2 Pages

    Blood grouping is a test to determine blood group of a person. Before blood transfusion or if you plan to donate blood, the test is important. Blood A cannot mix with blood B or blood AB so blood group is important to be known.A dangerous immune response will occur if receive blood that is not compatible with own blood type. The human immune system will destroy the incompatible blood type.

    Read More

More about Hemochromatosis Research Paper

Open Document