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Hemophilia - College Essay

Hemophilia


is a genetically inherited bleeding disorder which is caused when one of the plasma proteins (needed to clot) is missing or abnormally formed in the blood. The word comes from the Latin word hemo, meaning blood and the word philia, meaning: having a tendency towards. Knowledge of has been around since biblical times (due to the age of it is uncertain who the exact founder of the disease is) but it wasn't until the 1960's that scientists began to make new advances towards figuring out what was. There are two types of : A or factor VIII deficiency, and B or factor IX deficiency. A is more common than B with 85% of those affected by having it.
A person with does not bleed ...

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, although B is 5 times less common that A. All races, religions, and economic groups are affected by .
is a bleeding disorder which is inherited genetically. Due to the pattern of inheritance, the disorder generally affects males only. About one third of cases come with a previous family history. Women with a hemophilic gene are called carriers while men are either cs or normal. A daughter of a mother who is a carrier and a father who is normal has a 50% chance of being a carrier herself. A son of the same mother and father has a 50% chance of having . Most of the time carriers are not affected by the disease, but sometimes there are minimal symptoms. Many times is hidden for many generations if no affected males are born. Therefor the hemophilic gene is carried through many generations of females who, because they have one X chromosome that is normal, do not suffer from the disease themselves. Other cases may have no family history, which would mean that the change ...

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"Hemophilia." Essayworld.com. June 6, 2004. Accessed November 28, 2024. http://www.essayworld.com/essays/Hemophilia/9039.
"Hemophilia." Essayworld.com. June 6, 2004. Accessed November 28, 2024. http://www.essayworld.com/essays/Hemophilia/9039.
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PAPER DETAILS
Added: 6/6/2004 09:16:13 AM
Category: Health & Medicine
Type: Free Paper
Words: 733
Pages: 3

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