Hemophilia Research Paper

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Hemophilia

Do you ever hate it when you bump it into something? No big deal right? Well that’s not quite the situation for people that suffer from Hemophilia. Hemophilia is a genetic disorder that is passed down from parents to their children. Problematic and frequent bleeding is the major aspect of this disorder, it is commonly detected before the victim reaches their adult years, but due to increased research there might be breakthroughs involving stem cell treatments.

The reason why people are born with Hemophilia is because they weren't born with an X chromosome. You inherit the X chromosome from your mother. This disease is sex-linked, because it only carries the X. It is more likely for males to have this genetic disorder, because the females are almost all carriers, though they can be affected as well. Hemophilia has some history behind, a royal history. Hemophilia has always been known as The Royal Disease. The queen of England Victoria was a carrier of this horrible disease. Only one out of her eight children, Leopold suffered from Hemophilia. Leopold suffered great loss of blood, from a bursting blood vessel. Most of the Royalty blood line either suffered or were carriers. …show more content…
Such manifestations can range from bleeding a lot from just a minor cut to blood in the urine. Another example would be bleeding in the joints, bleedings occur without you provoking it, with no obvious injury. Bleeding in the brain is very serious, for it can lead to long-lasting headaches, vomiting repeatedly, strange behavior, and suddenly feeling very weak. Seizure may also occur. For children, before the age of one year and six months it tends to be more severe. Toddlers are at more of a risk, because they tend to bleed into their tissues of their limbs. A small amount of bleeding, bruising, and lumps will appear, however there is a

Hemophilia Research Paper

Introduction 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…

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Hemophilia Research Paper

Hemophilia Michelle Karlson Millersville University Hemophilia is a rare and genetic blood clotting disorder affecting about 18,000 people in America today. It is a hereditary disorder that is passed from parent to child, normally from mothers to the sons. It can be carried by females and normally 1/4 of the children will have it. If a male has hemophilia, he cannot pass it on. However that will make his daughters…

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Factor IX Deficiency Hemophilia is a genetic disorder. It is a rare blood disorder causing the clotting of blood to take a long amount of time resulting in abnormal bleeding, or even bleeding that won’t stop. (Hemophilia). Males are most commonly affected by hemophilia and it is often passed down through families. Hemophilia B is the second most common type of hemophilia and it is similar to the most common type of hemophilia known as hemophilia A. Hemophilia B affects males but is known as…

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