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Which World Hemophilia Day is 2022?
Introduction to hemophilia Hemophilia is a group of hereditary hemorrhagic diseases, in which thrombokinase is damaged in the first stage of coagulation. It includes hemophilia A, hemophilia B and hemophilia C. Among them, hemophilia A is also called coagulation factor VIII deficiency or anti-hemophilia factor A deficiency. True hemophilia and anti-hemophilia globulin deficiency are traditional hemophilia; Hemophilia is also called coagulation factor ⅸ deficiency or plasma thromboplastin (PIC) deficiency; Hemophilia C is also known as coagulation factor VII deficiency and plasma thromboplastin precursor (PTA) deficiency. Among congenital hemorrhagic diseases, hemophilia is the most common, especially hemophilia A, accounting for about 85%, followed by hemophilia B and hemophilia C.
Genetic situation
① Male patients marry normal women, and the boys born are normal, while the girls are carriers.
② When a female carrier marries a normal man, the boy born may be a hemophiliac or a normal person, while half of the girls are carriers and half are normal people.
③ The probability that a sick man marries a carrier woman and gives birth to a boy is 50%, that is to say, about 1/2 of the boys born are normal. Among the girls born, there may be hemophilia or carriers.
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