Wait a second!
More handpicked essays just for you.
More handpicked essays just for you.
Hemophilia disease- health encyclopedia
Don’t take our word for it - see why 10 million students trust us with their essay needs.
Recommended: Hemophilia disease- health encyclopedia
Hemophilia is a genetic disorder that causes a person’s blood not to clot. This causes bleeding to continue without being stopped by blood clotting. The big issue of the disorder is when the person experiences internal bleeding, but only in some cases does this occur. There are different levels and types of hemophilia, but the main problem of blood not clotting is always present. Although a person can be treated so that they can live active, hemophilia may last for the person’s whole life.
The cause of hemophilia is when there is a mutation on the X chromosome. Different types of the disorder have different causes. For example, hemophilia A is when there is blood clotting in factor 8. Hemophilia B is result of factor 9 blood clotting and hemophilia
C is when there is blood clotting in factor 11. Different types of the disorder are inherited from a male or female parent to a male or female child. Hemophilia A and C are mostly passed down from mother to son because of the passing down of the X chromosome. Many daughters who receive it are just carriers. Hemophilia C can be from either parent and go to either child. Symptoms of hemophilia vary on the type of this disorder and the level it is at. Some of the symptoms can be mild and not really affect the victim. Others may experience severe bleeding that might be life threatening. Some symptoms include, bruising, swelling, a lot of bleeding, or random nosebleeds. Other results can be tight joints, blood in urine, or unusual bleeding after shots. Severe symptoms are, headaches, neck pain, sudden pain in joints, endless vomiting , or double vision. Treatments for hemophilia may be regular shots of DDAVP or clotting factor. This would just be daily medical infusion that would help blood clotting. The patient could also take blood clotting medicine or fibrin sealants that are placed on a wound or injury. Other treatments could be physical therapy or vaccinations. Options vary on which type of hemophilia a person has and on what level the disorder is. A possible future cure for hemophilia may not be so far away. There have already been experiments with this option and so far it has worked. This possible cure of the disorder is called gene therapy. A person with hemophilia can have certain cells taken out, depending on the factor of the disorder. Then, new genetic material can be inserted and in these cells, and placed back where they were. This new genetic material can tell the cells to produce for the factor of the disorder. This will get rid of the hemophilia and the symptoms will stop. The positive implications of this technology are that it will stop symptoms for those that are struggling with hemophilia. It has already been tested and has had a positive result so far. However, only animal tests have been completed and very few humans with positive outcomes. These tests have also not been determined on how long the treatment will last. The tests have not backfired so far but the possibility always stands. In conclusion, hemophilia is a genetic disorder that has been passed down and affected many humans over the years. Although some of the symptoms may be mild, there are many cases in which the disorder is life threatening. The possible issue of internal bleeding may put the person’s life in danger. However, with future technology, a possible cure may come. There are current tests for the cure of hemophilia and and results are showing that the end may not be far.
Originally thought to be an obscure illness, it was later identified as the most common genetic disorder for those with a Western European background. However, due to its low penetrance rate, only one out of two hundred are said to have the condition. Hemochromatosis is treated by the practice of bloodletting. It is one of the oldest treatments recorded in history, with its earliest records dating as far back as 3000 years ago in ancient Egypt. Routinely bleeding is beneficial as it not only reduces the iron in the bloodstream, but also combats issues such as heart disease and high blood
○ ABO incompatibility. People with an O blood type have antibodies that can attack blood cells in type A or B blood. If a mother 's blood type is O and her baby 's blood type is A or B, her antibodies may destroy the baby 's red blood cells and cause hemolytic disease.
Hemophilia is a genetic bleeding disorder. People who have hemophilia have a deficiency or an absence of a coagulation protein. A blood clotting factor is deficient or absent. Bleeding is most often in joints, such as the knee, elbow, or ankle, but bleeding can occur anywhere in the body. People with hemophilia bleed longer, not faster.
It only takes one abnormal gene for a child to have the disease for the rest of his or her life. The disease is a reoccurring cycle, and this rare blood disorder is rare to the minds that do not have the disease, and to the minds that have not studied the disease. Although there is no definite cure, a splenectomy will help maintain the disease. The million dollar question is “What is hereditary spherocytosis and is there a cure?” Hereditary spherocytosis is a disorder in the membrane of a red blood cell that causes the red blood cell to be shaped like spheres, instead of flat discs (Wint Carmella).
There is no cure for hemophilia yet but they can stop or keep the bleeding episodes from happening by injecting themselves with “purified clotting factors.” Additional treatment is necessary only if the purified clotting factors were attacked by the person’s immune system.
Haemophilia is used to describe a collection of hereditary genetic diseases that affect a mammal’s body’s capability to control thrombogenesis. Thrombogenesis is the way in which blood clots which is an important role in haemostasis. Two common forms of haemophilia are A and B. (1) Someone with A (otherwise known as classic haemophilia), clotting factor VIII is does not exist enough or is entirely absent. A person with haemophilia B (otherwise known as Christmas disease), clotting factor does not exist enough or is also entirely absent. Those with the disorder do not bleed a lot they just simply bleed for a longer period of time. All people with haemophilia A or B are born with the disorder as it is a hereditary disorder and passed down through generations very few cases of haemophilia are not genetic and are therefore rendered a spontaneous gene mutation which is then passed down.
Hemochromatosis, originating in people of Western European descent, is a disease that is still carried in the chromosomes of humans. Hemochromatosis is a hereditary disease that disrupts the way the body metabolizes iron. (Moalem, 2) A person who has hemochromatosis absorbs abundant amounts of iron. While mistaking the body for not having enough iron, it absorbs more that it needs, which causes piles of iron to form in the joints, muscles, and major organs. This buildup can cause liver failure, heart failure, diabetes, arthritis, infertility, psychiatric disorders, and cancer. When discovered by Armand Trousseau in 1865, it was looked at as extremely rare. (Doctors Lounge, post) Later on in history, it was discovered that many people with western European descent either carried or expressed the hemochromatosis gene. Statistics show 1 in 4 people with western descent carry the gene for hemochromatosis, but only 200 people of western European descent express the gene. (Mo...
Hemophillia is a rare bleeding disorder in which the blood does not clot normally. Hemophillia is usually inherited and people born with it have little or no clotting factor (a protein needed for normal blood clotting). These proteins work together with platelets to help the blood clot. When blood vessels are injured, clotting factors help platelets stick together to plug cuts and breaks on the vessels. Hemophillia usually occurs in males with about 1 in every 5 000 males being born with the disease each year. A hemophiliac does not bleed more intensely than a person without it but can bleed for a much longer time. In some severe cases, continuous bleeding occurs after minor trauma or can even happen spontaneously.They may also bleed inside their body(internally), especially in the knees, ankles, and elbows. The bleeding can damage organs and tissues and may be life threatening. There are two main types of hemophilia: A and B. People born with type A are missing or have low levels of clotting factor VIII (1 in 5 000 males). People born with type B are missing or have low levels of clotting factor IX (1 in 20 000 males). About 8 out of 10 people who have hemophillia have type A. The greatest concern for both types is deep internal bleeding and bleeding into joints. Hemophilia is a life long disease, but with proper treatment and self-care, most people maintain an active productive lifestyle.
Tsar Nicholas II and his Tsarina, Empress Alexandra, had only one son, Tsarevich Alexei. However, Alexei had inherited from his great-grandmother Queen Victoria the life-threatening genetic disease hemophilia B, a sex-linked genetic disease on the X chromosome that caused a condition of deficiency in blood-clotting and excessive bleeding, symptoms that usually remain hidden unless contracted by a male (Fuhrmann 37; King 28). To Nicholas II, it was imperative that he have a son to succeed him to secure the throne. Alexei was Nicholas’s sole male heir, giving Nicholas the incentive to protect his son at all costs. Without a scientific cure for the genetic disease, Alexandra turned to religion, namely Grigori Rasputin, a poor uneducated Siberian peasant to protect her son.
Over one million Americans in the United States are living with or have been diagnosed with leukemia. That’s a big amount of people. I chose to do my research paper on leukemia because two years ago I lost my grandma to the cancer. I wanted to know more about the disease and what was happening to her. I researched the different types, risk factors, symptoms, treatment, and what kind of research is being done to help cure leukemia. Leukemia is a cancer of the blood cells that start in the bone marrow. During leukemia the bone marrow starts to make a lot of abnormal white blood cells or “leukemia cells”.
Hemophilia is a rare genetic blood clotting disorder that primarily affects males. People living with hemophilia do not have enough of, or are missing, one of the blood clotting proteins naturally found in blood. Two of the most common forms of hemophilia are A and B. In persons with hemophilia A (also called classic hemophilia), clotting factor VIII is not present in sufficient amounts or is absent. In persons with hemophilia B (also called Christmas disease), clotting factor IX is not present in sufficient amounts or is absent. People with hemophilia do not bleed more profusely or bleed faster than normal; they bleed for a longer period of time.
Today i'm going to be talking about Hemophilia and the general overview of it. I will also talk about any potential cures. I will be talking about what Hempohilia can do to your body. I will also be talking about if theres a cure or just a treatment to make it less worse. I will also be talking about how people with Hemophilia deal with this disease. I will also explain how people will benefit from extended research on thi s topic. I’ll also talk about my personal opininon on this topic and what I think about it. So for my first question I’m explaining what the characteristics of Hemophilia are. The characteristics of Hemophilia are not very deadly but can be very annoying I’ll also explan the genetic causes of this disease.
Hemophilia is a serious genetic condition caused by a coagulation factor that causes a mutation in the f8 and f8 gene. Hemophilia can be treated but not cured. Further studies are currently being done today. Living with hemophilia can be very difficult .physical activity is not recommended for individuals living with this condition. Also surgery is highly dangerous because of the excessive bleeding. In society we have set backs but we have to learn to deal with them.
The genetic defect that causes albinism in other types of albinism is unknown, but it is speculated that it involves other enzymes used to make pigment. Albinism is passed from parents to their children through genes. For nearly all types of albinism, both parents must carry an albinism gene to have a child with albinism. Parents may have normal pigmentation, but still carry the gene. When both parents carry the gene, and neither parent has albinism, there is a one in four chance at each pregnancy that the baby will be born with albinism.
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.