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Abstract

Hemophilia is a genetic disorder inherited in an X-linked recessive pattern. Hemophilia is extremely rare among females (5). Although Hemophilia is passed down from the mother to children, in some cases, hemophilia occurs as the result of a spontaneous mutation. This occurs in approximately 30% of cases (6). A mutation of the F8 and F9 genes are responsible for Hemophilia A and B respectively.

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