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Taking a Look at Hemophilia

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Hemophilia is an inherited bleeding disorder that is passed from mother to son. This affliction is passed in such a way due to the fact that the gene that is responsible for hemophilia is carried on the X chromosome that the child receives from his mother. For someone to be afflicted by hemophilia means that their blood has a difficult time clotting. There people do not bleed any faster than the average person, they simply cannot stop bleeding once they start bleeding. As of this current moment, there are no known cures for hemophilia, but there are many treatments that are highly effective in helping to treat many of the issues associated with the bleeding disorder. (citation)
The discovery of hemophilia is something that is not credited to one single person. The discovery happened throughout the course of history with the findings of many doctors and researchers combined. There is evidence that hemophilia was first recognized as a bleeding disorder 1,500 years ago in the Babylonian Talmud. The Talmud is a collection of the findings of great Jewish scholars. While the scholars were able become aware of how this bleeding disorder was inherited and only afflicted the boys, they were not entirely sure of the fact that it was passed from the mother.
While the discovery of hemophilia is not credited to one single person, the revelation that there were two separate types of hemophilia was found by Alfredo Pavlosky, a doctor who resided in Argentina in 1944. Pavlosky realized

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