The Hemophilia Disease

To test for the diagnosis, you must get the testing done when you are first born or a person can get the disease when you are older so people may want to do a test every 10 years. The testing is done with a blood test they prick your finger to draw some blood and put the blood sample under a microscope to

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.

You are tested for this disease when you are pregnant and you are tested to see if your baby has this disease by getting blood drawn

The diagnosis can be made prenatally, but if not the diagnosis is made typically at birth.

Hemophilia, once called the royal disease is a problem with the clotting of blood. When a cut or bruise occurs it can bleed causing problems with people who suffer from hemophilia. Patients with hemophilia will continually bleed longer than a normal individual. This bleeding can lead to harmful levels of blood loss to internal bleeding. Hemophilia is very rare occurring once every five thousand people. Rare, however it is the most common x linked trait. When an injury occurs, blood cells called platelets plug the wound. Then fibrins seal it up. Hemophilia splits into two groups hemophilia A and hemophilia B. People who have hemophilia A have low levels of blood clotting factor 8. Hemophilia B patients have low levels of blood clotting factor

This disease is noticeable by the age of 6 to 12 months. Parental DNA pattern test is a test

“Hemophilia (heem-o-FILL-ee-ah) is a rare bleeding disorder in which the blood doesn 't clot normally.” (NIH, 2013) Hemophilia is a chromosome – linked bleeding disorder caused by

Hemophilia is a possible cause of unexpected bleeding during surgery. This paper will discuss important topics related to hemophilia, including pathology, risk factors, signs and symptoms, and treatment.

Megan is a 30yo, G2 P0010, who was seen for a consultation due to her history of seizures. She has had seizures since she was about 8 years old and is currently on Lamictal. She was on 600 mg daily but did have a seizure about 3 weeks ago and was seen by her neurologist and her Lamictal was increased to 800 mg daily. She has not had a seizure in the past 3+ weeks. Overall on today’s assessment she has no complaints.

Alexandra did little to dispel growing discontent for her husband. She ruled side by side with her extremely influential friend, Grigory Rasputin. Rasputin was the only person able to treat the hemophilia of her only son, Alexis, heir to the Russian throne. Rasputin’s close relationship to the Empress allowed him to gain his own sense of power. He quickly began dismissing efficient ministers and appointing incompetent ministers solely on whether or not they supported him. Nicholas began to be seen as a man who willingly let his incompetent wife run the government, while he attempted to regain his pride on the western front. Conservatives began to plot against Nicholas in order to save their monarchy.

Hemophilia A is distinguished by extreme bleeding into soft tissues of the body known as hematoma, and bleeding into joint spaces known as hemarthroses. Hemarthroses lead to severe condition known as hemarthropathy. Repeated episodes of hemarthroses are very common to this disease. The severity of hemophilia A symptoms is directly proportional to factor VIII blood level and is classified as mild, moderate and severe.

Hemophilia is a lot more than just a cut that doesn’t stop bleeding. For starters, the word hemophilia is a combination of the Greek words for “blood” and “love”, which is a way of saying people with hemophilia “love to bleed”or just can’t stop to blood. Why is that? A large part about the disease comes from the effect it has on the cardiovascular system, but more importantly the hemostasis of the body. Normally, when damage occurs to a blood vessel walls, there’s an immediate narrowing of the blood vessel which limits the amount of blood flow. Which leads for some platelets adhere to the damaged vessel wall, and become activated that then recruit additional to form a plug. This platelet plug is the result of the primary hemostasis. Leading up to the coagulation cascade to be activated. In 2010, Chris Pallister and Malcolm Watson best summarized coagulation cascade as:

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.

Hemophilia (sometimes spelled haemophilia) is a rare genetic blood disorder which prevents blood from clotting normally. There are two types of hemophilia, and they are hemophilia A and hemophilia B. Hemophilia A is also called classic hemophilia, and is caused by a mutated or missing factor VIII, which is a clotting protein. Hemophilia B is sometimes called Christmas disease, because the disorder was first reported in a patient with the last name Christmas. Hemophilia B is caused by a mutated or missing factor XI, which is also a clotting protein.

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.