Hemophilia Research Paper

Hemophilia is a condition where a person's blood is unable to clot properly. This condition can make a simple dental procedure more risky. People who have hemophilia will also have a harder time healing after a dental procedure. You definitely want to let your dentist know if you have hemophilia.

Hemophilia is an X-linked recessive disease in which blood lacks blood-clotting proteins. Females have two X chromosomes, indicating that they are generally carriers and transmit the gene to their sons. People with mild hemophilia bleed after surgery, injury, or trauma. Severe hemophilia produces spontaneous internal bleeding in joints and muscles. Fortunately, medicines and lifestyle changes offers hemophiliacs fairly normal lives. Through learning about hemophilia, I became interested in genetic diseases and finding a cure for those

According to the National Hemophilia Foundation (.n d.), people with VWD experience recurrent nosebleeds, easy bruising and extreme bleeding for the duration of and after invasive procedures, such as tooth removals and surgery. Women often experience menorrhagia, heavy menstrual periods that last lengthier than usual, and hemorrhaging after giving birth. The signs and symptoms depends on the severity of the disease.

The genetic disorder of Hemophilia is where the clotting factors of the blood are absent or deficient, causing it to be a dangerous disorder to the people who have it. This disorder is where the people who have it will bleed easily and accessibly. Different types of hemophilia are classified by different deficient clotting factors in the blood. Treatments for hemophilia are available, including transfusions of frozen

Hemophilia A is an X-linked disorder caused by a deficient or defective clotting factor VIII (FVIII) protein, and characterized by spontaneous or traumatic bleeding into joints and muscles [Ragni]. It causes afflicted individuals to not be able to coagulate their blood very efficiently or at all when getting an injury in which blood is exposed either internally or externally. This disease can be very dangerous and fatal because major blood loss can occur if the patient has not received treatment.

The Arab physician Albucasis, who lived in the 12th century, wrote of a family whose males died of bleeding after minor injuries. Then, in 1803, a Philadelphia physician named Dr. John Conrad Otto wrote an account of a hemorrhagic disposition existing in certain families '. He recognized that the condition was hereditary and affected males (Society). The diagnosis of hemophilia is actually quite simple. Blood labs are drawn if a doctor suspects their patient to have a bleeding disorder. Blood tests will indicate what percentage of clotting factors are present in the blood. There are three types of hemophilia.

Hemophilia is an inherited bleeding disorder that is passed from mother to son. This affliction is passed in such a way due to the fact that the gene that is responsible for hemophilia is carried on the X chromosome that the child receives from his mother. For someone to be afflicted by hemophilia means that their blood has a difficult time clotting. There people do not bleed any faster than the average person, they simply cannot stop bleeding once they start bleeding. As of this current moment, there are no known cures for hemophilia, but there are many treatments that are highly effective in helping to treat many of the issues associated with the bleeding disorder. (citation)

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 50-150% of the normal level of factor VIII or IX. There are about 20,000 hemophilia patients in the United States. Each year, about 400 babies are born with this disorder. Approximately 85% have hemophilia A and the remainder has hemophilia B.

Severe hemophiliacs can also have frequent nosebleeds, blood in their urine (bleeding in their kidney and bladder), and blood in their feces(from bleeding in their intestines and stomach).

However, the head bleeding common with hemophilia might occur under the skin or inside the skull leading to persistent headache, seizure, ears or nose bleeding, visual problem, vomiting, dizziness or even difficult walking or unstable gait. Other bleeding areas are the spine, and gastrointestinal bleeding (stomach and intestines). Bleeding in the spine may cause urination difficulty or bowel movement impairment. GI bleeding signs and symptoms include; bloody or black emesis, and red or black stool. Immediate medical attention is needed when these severe cases of bleeding are noted (rarebleedingdisorder.com).

Bleeding disorders constitute a wide range of disorders in which the patients tend to bleed excessively. Such bleeding may be severe, with bleeding episodes starting in early childhood, or mild, discovered after a haemostatic challenge like surgery, dental procedures, or trauma. The bleeding symptoms may range from nosebleeds, easy bruising or heavy menstrual periods to bleeding into joints, muscles and deep

Hey do you know what hemophilia is? Well it's a bleeding disorder, when you bleed too much when having an injury making you have too much blood loss. There are treatments that can help you if you have Hemophilia ,but sadly we have no cure for it yet. When you have Hemophilia you have to stay away from things that can hurt you like when you are reading a book you have to be careful because you don't want a paper cut.The treatments that can help you when you have replacement therapy, replacement therapy is a treatment aimed at making up a deficit of a substance normally present in the body.

The definition of hemophilia is that it’s a rare disease housed in the body. What happens is the blood does not clot normally due to the fact it lacks the sufficient blood-clotting proteins. Also, when having this disorder of hemophilia, the person can bleed for a longer period of time after a wound of cut. Depending on the person with hemophilia so small cuts or injuries for the most part do not become much of a problem in their day to day lives. In most cases the risk comes in when there is deep bleeding inside the body, especially in the knees, ankles and elbows and most times this can appear as bruising. This type of injury can lead to damaged organs and tissues, and for the most part can

Hemophilia is a bleeding disorder. That slows the blood clotting process. People that have Hemophilia bleed extremely after, having an injury,surgery, or just falling down. Serious complications be very dangerous because, it can start bleeding into joints, muscles, brain, and other internal organs. People with mild complications of Hemophilia usually don’t bleed spontaneously, but they won’t bleed spontaneously, until a surgery or serious injury.

Hemophilia is a problem with the blood in a person that causes them to bleed not any faster than normal, but they often bleed for a longer period. Their blood is missing the clotting factor (a protein in the bloodstream that works to control bleeding). Hemophilia is quite rare; roughly 1 in every 10,000 persons are born with it. Rarely, hemophilia can be an acquired disease which just means a person is not born with it, but will develop it during their lifetime. This rarity occurs when a person's immune system forms antibodies that attack the clotting factor in the blood. The entire antibody population fights against the blood to prevent the clotting factors from working properly.