Hemophilia is a sex-linked hereditary bleeding disorder in which it takes a long time for the blood to clot and abnormal bleeding occurs. It is a hereditary blood coagulation disorder caused by a deficient activity of plasma protein factor thirteen and nine, which affects the clotting property of blood. A coagulation disorder is a disorder associated with platelets- blood cells essential for blood clotting. The platelets don't function properly in the body of hemophiliacs. There are two types of
Hemophilia Hemophilia is a hereditary bleeding disorder. (1, 36)(2, 759)(3, 529)(5, ____) (6) (7) (8) (10) (12) (13) (14) Hemophilia is a disease where the blood does not clot normally. (1, 36)(3, 529)(2, 759)(5,____)(6)(10)(13) “Hemo” means blood and “philla” means a tendency towards.(6)(7) In most people when they get a cut the platelets plug the hole and release chemicals which attract proteins and activate proteins found in the blood that are known as clotting factors.(6) The proteins
Hemophilia Hemophilia is the oldest know, lifelong bleeding disorder(“Hemophilia”2004). It is named for two inherited diseases in which the blood does not clot normally. Several different plasma proteins must be present for blood to clot property. If one of the plasma proteins is missing, or present at low levels, blood clots very slowly(“Hemophilia” The Marshall Cavendish). The two most common types of hemophilia are: Hemophilia A or FactorVIII(8) deficiency and Hemophilia B of FactorIX(9) deficiency(“Hemophilia”
Hemophilia Manitoba Hemophilia Manitoba, or hemophilia, is a sex-linked genetic disorder that is effecting about 20,000 Americans, most of which males. A person with hemophilia either has an inactive or inadequate supply of one of several blood factors needed for blood to clot. Because of this hemophilia can be mild, moderate, or severe. Severe hemophiliacs are at risk for bleeding during surgery, trauma, or even dental work. There are two types of hemophilia, A and B (Christmas disease). Hemophilia
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
Hemophilia is the oldest known hereditary bleeding disorder. There are two types of hemophilia, A and B (Christmas Disease). Low levels or complete absence of a blood protein essential for clotting causes both. Patients with hemophilia A lack the blood clotting protein, factor VIII, and those with hemophilia B lack factor IX. A person with severe hemophilia has less than 1% of the normal amount of a clotting factor - either Factor VIII (8) or Factor IX (9). People without hemophilia have between
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 into joints, such as the knee, elbow, or ankle, but bleeding can occur anywhere in the body. People with hemophilia bleed longer, not faster. The severity of hemophilia varies greatly. Hemophilia A and Hemophilia B are the most common genetic bleeding disorders. Hemophilia A is observed in 80 percent
The genetic disorder which I have chosen as the subject of my report is hemophilia. There are two types of hemophilia, hemophilia-A and hemophilia-B. The clinical symptoms of both are very similar so for the purposes of this paper I have chosen to concentrate on hemophilia-A. Hemophilia-A is an X linked bleeding disorder resulting from a defect in a protein known as coagulation factor VIII. Since the disorder is X linked it is expressed mainly in males, who must have mothers who are carriers. Females
to our sociable needs. But this can also affect modern medicine, political factors, economic, and societal balances in our nation. For medicine, Biotechnology has been a blessing, healing people who suffer from a sex-linked trait known as Hemophilia. Hemophilia is a condition where the person may die of blood loss when cut or wounded. This is caused by a lack of a certain chemical known as Factor 9, which allows the patient to heal from wounds. Scientists may now insert a gene into the patients own
Hemophilia Severe bleeding. That's what happens when a person has Hemophilia. "More than 25,000 people in the United States have Hemophilia" (Description of Hemophilia 1). "Hemophilia is an inherited deficiency of a blood-clotting factor that results in episodes of dangerous bleeding" (Hemophilia 1). As you read through this essay, you will learn more about the disease. Some characteristics should be. First you will learn about the diagnosis and prognosis of Hemophilia. Second you will
1) Hemophilia is an inherited disorder in which somebody who is born with it has very minimal or no clotting factor at all. It is a very rare condition, with only about 20,000 men who have it in the United States. Clotting factors are special proteins that are inside the blood that help it clot. Without them, or having very minimal like a hemophiliac, results in prolonged or non-stop bleeding after receiving an injury. It can also result in internal bleeding in joints, tissues, and muscles. 2) In
reason is because of hemophilia. In order to understand this common genetic disorder, it is helpful to know what it is, what symptoms or treatments to look for, and how it is treated. First of all, we need to know that hemophilia is a bleeding disorder that slows or prevent the process of blood clotting properly. Not only this, but we need to know there are 2 types of hemophilia, hemophilia A, and hemophilia B. To begin, lets find out how Hemophilia A and B are different. Hemophilia A is more common
People who have hemophilia have little to no clotting factor. This disease is almost always inherited and is rarely ever developed during someone’s lifetime. Hemophilia comes in two types, A and B. It is more common in males rather than females but can be carried by females. Also known as Von Williebrand Disease (VWD), it is named after Dr. Erik Von Williebrand who assessed the disease differently in Helsinki, Finland in 1924. Without treatment, people with hemophilia die before they reach adulthood
throne he married Princess Alix of Hesse-Darmstadt. Alix became the Grand Duchess of Russia. Her name was changed to Alexandra. Her religion was also changed to Russian Orthodox (King 77). The Czar and Czarina had 5 children. The youngest, Alexis had hemophilia. He was to be the next ruler of Russia, but unfortunately, the day never came (McGuire 31). During the late 1800’s and early 1900’s, Russia’s government began to decline. Czar Nicholas went against his advisor’s advice and led the Russians through
organisms DNA and creating a new organism with this same DNA. The new organisms will be physically identical to the original organism. Somatic cell manipulation is simply injecting new genes into somatic cells in order to cure a disease such as hemophilia. Germline manipulation is altering the genes in sex cells that are passed onto offspring, so that the offspring will posses certain specific characteristics. From the descriptions of these few processes, it can be seen why genetic engineering has
first mammal (sheep), named Dolly, from an adult cell (Wilmut, 21). Since the first cloned mammal, scientists have worked to find a practical application for cloning that will produce advances for human diseases. In some inherited disorders, such as hemophilia, cystic fibrosis and emphysema, the only way to treat such patients is through therapeutic proteins, which are obtained through the milk of an animal (Straight). These animals carry a certain protein that is secreted in their milk or blood, which
Ivan the Terrible was stricken with disease, and driven mad. During the "exploration" of the new world, Cortes's greatest ally against the Aztecs was smallpox. Napoleon's Grand Army was defeated by the Russians, and typhus. Queen Victoria spread hemophilia to her heirs, leading to the illness of the only son of Czar Nicholas, and the fall of monarchy in Russia.1 All the events are horrible in every way, but have struck a chord with people around the world. Perhaps it is our inherent morbid curiosity
Hemophilia There are many blood disorders and one of them are hemophilia."Hemophilia is a rare disorder in which your blood does not clot normally, because it lacks sufficient blood-clotting protein"(mayoclinic.org). In normal blood, proteins called clotting factors work together to format a clot whenever bleeding takes place. Someone with hemophilia has a shortage and/or does not have enough of a certain clotting factor, so the blood can not make a clot. "Hemophilia has an impact on one in five
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
When the potential to form a blood clot is dangerously decreased this is know as Hemophilia. Bleeding out could occur from the most minor of cuts when people have Hemophilia. Over bleeding from scraping your skin is the largest indicator. It is a pretty uncommon disorder but there are a few types. The most heard of are Type A and Type B. According to Medical News Today, Type A is defined as a lack of the clotting factor eight. Type A is also responsible for around ninety percent of these accounts