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14 answers

Its Hemophilia.

Hemophilia is a genetic bleeding disorder that prevents the blood from clotting normally. The main symptom is uncontrolled, often spontaneous bleeding. Internal bleeding into the joints can result in pain, swelling and, if left untreated, can cause permanent damage.

take a look at the National website...
http://www.hemophilia.org/NHFWeb/MainPgs/MainNHF.aspx?menuid=0&contentid=1

2007-02-06 13:40:49 · answer #1 · answered by thebe_gl 3 · 0 0

hemophilia a is the most common type of hemophilia. It is also known as factor VIII deficiency or classic hemophilia. It is largely an inherited disorder in which one of the proteins needed to form blood clots is missing or reduced. In about 30% of cases, there is no family history of the disorder and the condition is the result of a spontaneous gene mutation.



Approximately one in 5,000 males born in the United States has hemophilia. All races and economic groups are affected equally.

When a person with hemophilia is injured, he does not bleed harder or faster than a person without hemophilia, he bleeds longer. Small cuts or surface bruises are usually not a problem, but more traumatic injuries may result in serious problems and potential disability (called "bleeding episodes").

There are different levels of hemophilia: mild, moderate, and severe:

• People with mild hemophilia (6% to 49% factor level) usually have problems with bleeding only after serious injury, trauma, or surgery. In many cases, mild hemophilia is not discovered until an injury or surgery or tooth extraction results in unusual bleeding. The first episode may not occur until adulthood.

• People with moderate hemophilia, about 15% of the hemophilia population, tend to have bleeding episodes after injuries. They may also experience occasional bleeding episodes without obvious cause. These are called "spontaneous bleeding episodes."

• People with severe hemophilia, about 60% of the hemophilia population, have bleeding following an injury and may have frequent spontaneous bleeding episodes, often into the joints and muscles.


Everyone inherits two sex chromosomes, X and Y, from his or her parents. A female inherits one X chromosome from her mother and one X chromosome from her father (XX). A male inherits one X chromosome from his mother and one Y chromosome from his father (XY). The gene that causes hemophilia is located on the X chromosome.

A woman who gives birth to a child with hemophilia often has other male relatives who also have hemophilia. Sometimes, a baby will be born with hemophilia when there is no known family history. This means either that the gene has been "hidden" (that is, passed down through several generations of female carriers without affecting any male members of the family) or the change in the X chromosome is new (a "spontaneous mutation").

There are four possible outcomes for the baby of a woman who is a carrier. These four possibilities are repeated for each and every pregnancy:
1. A girl who is not a carrier
2. A girl who is a carrier
3. A boy without hemophilia
4. A boy with hemophilia

With each pregnancy, a woman who is a carrier has a 25% chance of having a son with hemophilia. Since the father's X chromosome determines the baby will be a girl, all the daughters of a man with hemophilia will be carriers. None of his sons, which is determined by the father through his Y chromosome, will have hemophilia.



Genetic counseling is available at most HTCs. These professionals have information to help you make family planning decisions.

In general, small cuts and scrapes are treated with regular first-aid: clean the cut, then apply pressure and a band-aid. Individuals with mild hemophilia can use a non-blood product called desmopressin acetate (DDAVP) to treat small bleeds. Deep cuts or internal bleeding, such as bleeding into the joints or muscles, require more complex treatment. The clotting factor missing (VIII or IX) must be replaced so the child can form a clot to stop the bleeding.

2007-02-06 13:40:17 · answer #2 · answered by unknownnnnn 2 · 0 0

Hemophilia. It's a genetic disease.

2007-02-06 13:38:38 · answer #3 · answered by Anonymous · 0 0

there are two different types of bleeding disorders. its either von Willebrand Disease or hemophilia

2007-02-06 13:40:41 · answer #4 · answered by jane 2 · 0 0

hemophilia is a disease where the blood lacks its ability to clot.

2007-02-06 13:48:05 · answer #5 · answered by Amy M 2 · 0 0

Hemophilia, it's genetic, i know some people who have it like my friend's mom.

2007-02-06 13:39:07 · answer #6 · answered by Anonymous · 0 0

VWD - or - von Willenbrand Disease

2007-02-06 13:40:24 · answer #7 · answered by T D 3 · 0 0

hemophilia, but it's more present in young caucasian boys than any other demographic.

2007-02-06 13:39:35 · answer #8 · answered by Dr. PHILlis (in training) 5 · 0 0

1st 3 right

2007-02-06 13:39:18 · answer #9 · answered by Anonymous · 0 0

low iron can also cause bleeding

2007-02-06 13:39:16 · answer #10 · answered by upnorth 2 · 0 0

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