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There is no "cure" for haemophilia, only treatment with the appropriate clotting factors.

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Haemophilia (also spelled hemophilia) is genetic disorder. It is more licely for a male to get it than female.

About one of 5,000-10,000 male babies are born with Haemophilia A. About one of 20,000-34,000 male babies are born with Haemophilia B.

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Haemophilia is a genetic disorder. Usually males are the victims and females are carriers of this disease.

There is no prominent cause of this disease but now-a-days it is seen that the families which do not have any history of haemophilia may also have a haemophiliac child. The reason for this is that sometimes there is mutation at genetic level which may lead to deficiency of clotting factor(VIII OR IX) in the blood of the child resulting in haemophilia.

One may also suffer from haemophilia at a very later stage of his life but that is very rare. This is the case of Acquired Haemophilia.

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Haemophilus is not a STD.

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i believe all types of haemophilia are genetic although i am not sure. but i do know that CLASSIC HAEMOPHILIA is a genetic disorder

Haemophilia A and B are both genetic. Haemophilia A (which is the most common) occurs when your blood lacks a clotting agent called factor 8. Haemophilia B occurs when you lack factor 9 in your blood. There is also acquired Haemophilia, this occurs when the immune system starts attacking clotting agents within the blood, this usually occurs in elderly people. Both forms of genetic haemophilia mostly occur in males, it rarely occurs in females. Unfortunately there is no cure but it is quite easily controlled with injections of the missing clotting agent.

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Haemophilia It's Not What You Think - 1990 V is rated/received certificates of:

Australia:G

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Ribbans, W. J. "Orthopedic Care in Haemophilia." Hospital Medicine 64, no.2 (2003): 68-69.

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Colourblindness or haemophilia

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The classical spelling of hemophilia is haemophilia.

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There are several symptoms of haemophilia. Among them are adverse reaction to clotting treatment, joint damage, deep internal bleeding, transfusion transmitted infection, and intracranial hemorrhage.

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Yes, it is an inherited disease, you can not catch it.

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One example of a sexually influenced trait in humans would be haemophilia. The gene responsible for haemophilia is located on the X chromosome, and if a man receives a gene from his mother (men's X chromosomes always come from their mother) that is positive for this trait, he will exhibit haemophilia. Women must have two X chromosomes that are positive for haemophilia in order to exhibit the trait, because it is a recessive gene.

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Haemophilia is a congenital disorder, those that have it were born with it and it manifests early in life.

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He suffered from haemophilia, an inability of his blood to clot correctly.

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* Hydrolysis * Haemophilia * Hiccup * Horizontal * Haggard * Hypocirsy

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Haemophilia A - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor VIII

Haemophilia B - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor IX

Haemophilia C - an inhibition of clotting caused by a deficiency in a protein called Clotting Factor XI

-similar to-

vonWillebrand's Disorder - an inhibition of clotting caused by a deficiency in a protein called the vonWillebrand's Factor

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Hemophilia is a genetic disorder that is usually inherited in an X-linked recessive pattern. It can appear to skip a generation when a carrier female passes the gene to her son, who then expresses the disorder. However, it doesn't truly skip a generation as the gene is passed on in each generation.

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Haemophilia suffer mainly men, since they hemophilia genes are permanently activated.

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There are several such diseases. The most well known is hemophilia.

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G M. Broadhead has written:

'Treatment of haemophilia'

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Here are some causes of bleeding disorder:

1. Thrombocytopaenia

There is a deficient number of circulating platelets. Petechiae appears due to spotaneous, widespread haemorrhage. It can be treated with transfusion of concentrated platelets.


2. Impaired liver function

The liver does not have the ability to synthesise procoagulants. This eads to vitamin K deficiency, hepatitis, and cirrhosis.


3. Haemophilia

It includes several similar hereditary bleeding disorers. Haemophilia A is the most common type of haemophilia and it occurs due to factor VIII deficiency. Haemophilia B is due to factor IX deficiency. As for haemophilia C, this condition is mild and occurs to the the deficiency of factor XI.

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For most of the time yes, there is one instance where it doesn't, and that is Haemophilia If I am correct

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all of them are caused by genetic mutations

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A haemophilia patient should eat a balanced diet with a controlled portion of the protein.

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Gastrointestinal bleeding, haematuria, ecchymoses & subcutaneous heamatomas, epistaxis and prolonged bleeding from minor trauma.

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Georgi Filatov died on December 11, 1940, in Leningrad, Soviet Union of haemophilia.

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it may be caused by a bleeding disorder called haemophilia where your blood does not clot.

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No because her father and mother both did not have it, therefore it is impossible for her to have it

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Haemophilia(only if bleeding occurs)

leukemia

sickel cell anaemia

beta thalasemia

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Haemophilia(only if bleeding occurs)

leukemia

sickel cell anaemia

beta thalasemia

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  • The genes that contain the information for the cells to make the clotting factors 8 and 9 are located on the X chromosome
  • Women have two copies of the X chromosome (XX); those with a faulty clotting factor gene on one X chromosome and a working copy on the other partner X chromosome are genetic carriers for haemophilia and would not usually be affected
  • Males have only one X chromosome and a Y (XY); those with a faulty clotting factor gene on their X chromosome will have haemophilia as they have no working gene copy on the Y chromosome
  • For men and women to have the same amount of genetic information produced in their cells, one X chromosome copy is usually randomly 'switched off' or inactivated in a woman's cells. In about 10% of women who are genetic carriers for haemophilia, this 'switching off' system results in more of her cells containing the active X chromosome carrying the faulty clotting factor gene copy than the working copy, so she may be mildly affected with haemophilia

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If you mean where in the body, it keeps the blood from clotting normally. If you mean in the world . . . try Google!

http://en.wikipedia.org/wiki/Haemophilia

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Coagulopathy is a clotting and bleeding disorder where the blood struggles to clot. Coagulopathy may be caused by genetics, such as haemophilia or another disfunction.

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Because Stephen Christmas was the first person diagnosed with it .and it was released in Britain for first time on christmas day

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Haemophilia is often spelled with an extra "a" in scientific journals but hemophilia has become widely used.

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Haemophilia is a health condition where the blood cannot clot as it should normally, for cuts and wounds. As it can not clot, it is very difficult to stop tye bleeding.

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Haemophilia (hemophilia) is a disease where the blood does not clot and any cut can lead to fatal bleeding.

See the Related Link.

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Hemophilia is more common in males. It's a sex-linked disease.

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Haemophilia is a genetic disorder and is not contagious. In the specific case of Tsarevich Alexei it was passed to him from his mother Alexandra, and can be traced back to Queen Victoria.

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Hemophilia itself is not a secret but hemophiliacs themselves may not choose to reveal their diagnosis because of its association with HIV which is still widely misunderstood and biased against.

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Victoria was the first known carrier of haemophilia in the royal line.

http://en.wikipedia.org/wiki/Queen_Victoria#Within_Britain

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The gene for haemophilia is located on the X chromossome, and can be passed by haemophiliac or carrier mothers to sons (more common) or daughters. Haemophiliac fathers will always have carrier (but not necessarily affected daughters.)

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"Like most recessive sex-linked X chromosome disorders, haemophilia is more likely to occur in males than females. This is because females have two X chromosomes while males have only one, so the defective gene is guaranteed to manifest in any male who carries it. Because females have two X chromosomes and haemophilia is rare, the chance of a female having two defective copies of the gene is very remote"

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