Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
There are no hard answers to this, it depends strictly on luck. The statistics are though not very good for their children. Statisically the couple have a chance of having a normal son, a daughter that is a carrier for hemophilia, a daughter with hemophilia and a son with hemophia.
50 million ppl have hemophilia
No, Hemophilia is a genetic disease. A person is born with it.
Her father has to have hemophilia as well, and the mother is a carrier or also has hemophilia. So if we pretend that the hemophilia gene is "x", you need to have "xx" to have hemophilia. The father must have the genotype "Yx" and the mother has the have "Xx" or "xx".
Hemophilia is treated by replacing the missing clotting factors intravenously.
Hemophilia is treated by replacing the missing clotting factors intravenously.
Gene replacement therapy
replace the clotting factor in the veins
A: Treatment of hemophilia involves replacement of factor VIII chronically, with additional doses administered during phases of acute bleeding. Patients with mild hemophilia A can sometimes be treated with a synthetic hormone called desmopressin. Desmopressin stimulates the release of the carrier for factor VIII, thus causing increases in blood concentration of factor VIII.
Hemophilia is one disease in which blood does not clot normally. von Willebrand's Disease
There is no chance that the child will have hemophilia even if the spouse has hemophilia. Any girls the couple has will be carriers if the spouse has hemophilia.
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MedicinesPhysical therapySpeech therapyOccupational therapySwallowing therapy
Can anyone be a candidate for the hemophilia a
Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
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