Hemophilia A/B (Royal Disease)
Introduction
Have you ever wondered about diseases? Today’s disease is called Hemophilia. Hemophilia has many symptoms, problems, and medical treatments. Hemophilia was discovered by Dr. Judith Pool. Hemophilia is a rare disease. It prevents cuts and wounds from getting clotted properly. “The platelets are not sticky enough for the wound to be sealed”. This disease usually leads to lots of blood loss. There is no cure, but there are treatments. “There are two types of Hemophilia, Hemophilia A and Hemophilia B one being rarer than the other.” “The way you get Hemophilia is if your parents had it and you inherited it”. Hemophilia is called the “Royal Disease” it dates back to 1800’s when Queen Victoria was queen. She then passed the disease to her daughters. “When the daughters decided to get married and have children they then passed the disease to their children and husband which then spread like crazy.” Which today it is known as hemophilia. What does Hemophilia do to the body
Hemophilia does many things to the body especially when you get a cut or a bruise. First of all you body is trying to send platelets to the wound to seal it up and heal it, but it can’t the platelets are not sticky enough. Second if you’re platelets aren’t sticky enough it will let the
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Listing from blood in the urine to nosebleeds and many others. More symptoms include deep bruises, blood in stool, excessive bleeding, pain in joints, and tight joints. Hemophilia is usually inherited which means that the parents pass the disease to their offspring. It is caused by a pairing up with a hemophilia gene if the mom has a normal clotting and the dad doesn’t he has the hemophilia gene. However if they have a child the child will not have hemophilia because the mom is dominant over the dad. It would be a genetic tendency because the mom and dad have genes that will join together and determine to see if their child will have
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
She married my grandfather who was one of four children, all boys, none of whom were affected by any disease that anyone is aware of. My grandparents had two children, my mother and my uncle. My uncle has hemophilia but my mom doesn’t. My uncle married my aunt (who is unaffected) and they had two children, neither of whom showed any sign of any disease. Their boy is still single but their girl got married, to a normal man, and had a son, who has hemophilia A.
As the best of my knowledge I believe the two year old child is suffering from an inherited disorder called hemophilia. The Mayo Clinic describes hemophilia as a rare blood disorder that lacks sufficient blood clotting proteins. (Staff, B.M. ((n.d.)). Hemophilia. Retrieved September 27, 2016, from http://www.mayoclinic.org/disease-conditions/hemophilia/basics/treatment/con-20029824
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
Meyers, R., W. Adams, K. Dardick, J. Reinisch, F. Reyn, T. Renna, and O. McIntyre. "The Social and Economic Impact of Hemophilia--a Survey of 70 Cases in Vermont and New Hampshire." The Social and Economic Impact of Hemophilia--a Survey of 70 Cases in Vermont and New Hampshire. American Journals of Public Health, 1 Apr. 1972. Web. 30 Aug. 2015. .
According to the CDC website, Hemophilia, is a hereditary bleeding disorder which affects mostly males due to X chromosome singularity. Hemophilia is a medical condition in which the blood clotting becomes a challenge for those affected. Symptoms include spontaneous bleeding from injuries or surgery. Blood contains many proteins called clotting factors that assist in blood coagulation, however; those individuals with hemophilia have low levels of either factor VIII or factor IX. The severity of the condition is determined by the amount of factor in the blood thus the lower the amount of the factor, the higher the chances that spontaneous bleeding will occur leading to more severe health complications.
A genetic disorder that affects the blood vessels when injured that results in clotting is Hemophilia. This inherited disorder is not contagious and is found through various lab tests such as a blood clotting test. The way someone can be aware if they could encounter Hemophilia is simply by viewing their medical history,
Hemophilia is a rare disorder in which your blood doesn 't clot normally because it lacks sufficient blood-clotting proteins known as clotting factors. Hemophilia is an inherited (genetic) disorder. There 's no cure yet. But with proper treatment, most people with hemophilia can maintain an active, productive lifestyle. Hemophilia was recognized, though not named, in ancient times. The Talmud, a collection of Jewish Rabbinical writings from the 2nd century AD, stated that male babies did not have to be circumcised if two brothers had already died from the procedure.
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.
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.
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.
Attention Getter: About 400,000 people are living with hemophilia, a rare blood disorder that causes blood to clot abnormally. Many of these people also develop HIV and AIDS, an immune deficiency. Even more shocking is the 78 million people living with HIV. All of these conditions are lifelong and fatal. Over 40 million people each year die of HIV or hemophilia. What 's even more terrifying is the amount of misinformation pertaining to these subjects, such as the difference between HIV and AIDs, and the causes of these conditions.
Hemophilia or the “royal disease” had a huge affect on history. Hemophilia is an X-linked recessive disorder which lacks the ability to to properly form blood clots. So small cuts and bruises could be fatal for people with the disease. Hemophilia is called the “royal disease” because it spread through the royal families of Europe. This started in 1837 when Queen Victoria became queen of England. Queen Victoria had the hemophilia gene which she passed to her children who passed to the ruling families of Russia, Spain, and Germany. Her daughter Alice was a carrier and she had a daughter Alix who was also a carrier. In 1894 Alix became Empress Alexandra when she married Russia’s Czar Nicholas. Then in 1904 they had a son named Alexis who had inherited hemophilia from Alexandra. Nicholas and Alexandra were very pre-occupied by their son’s serious health problems so a monk named Rasputin was the only person who was able to help Alexis. So, to relive Alexis pain, Rasputin used hypnosis. Nothing could make Alexandra stop believing that the welfare of her son depended on following the advice of Rasputin. But soon he also convinced her that both the welfare of Russia and the continued existence of the monarchy have also depended on him so now he controlled the royal family. Rasputin was murdered
The genetic disorder I chose to research was hemophilia. Hemophilia is a bleeding disorder where the blood doesn’t clot normally. It occurs, with rare exceptions, usually in men. The cause of hemophilia is a defect in the clotting factor VIII gene, located on the X chromosome. Hemophilia is hereditary also, meaning the children of a carrier, or someone with a mutated gene, may also get it. Some symptoms of hemophilia are excessive bleeding, both internal, which includes large bruises from bleeding into large body muscles, and external, which includes nose bleeds which occur for no apparent reason. Other symptoms are bleeding in the joints, brain, and gums.
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.