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Haemophilia A (or hemophilia A) is a blood clotting disorder caused by a genetic deficiency in clotting factor VIII, thereby resulting in significant susceptibility to bleeding, both internally and externally.
Haemophilia (British English), or hemophilia (American English) [6] (from Ancient Greek αἷμα (haîma) ' blood ' and φιλία (philía) ' love of '), [7] is a mostly inherited genetic disorder that impairs the body's ability to make blood clots, a process needed to stop bleeding.
Acquired haemophilia A (AHA) is a rare but potentially life-threatening bleeding disorder characterized by autoantibodies directed against coagulation factor VIII.These autoantibodies constitute the most common spontaneous inhibitor to any coagulation factor and may induce spontaneous bleeding in patients with no previous history of a bleeding disorder.
In honor of World Hemophilia Day, Yahoo Life spoke with two hematologists about hemophilia and common myths about the rare blood-clotting disorder.
Ryan White was born at St. Joseph Memorial Hospital in Kokomo, Indiana, to Hubert Wayne and Jeanne Elaine (Hale) White.When he was circumcised, the bleeding would not stop; when he was three days old, doctors diagnosed him with severe hemophilia A, a hereditary blood coagulation disorder associated with the X chromosome, which causes even minor injuries to result in severe bleeding.
Thomas Carine’s story of living an active life with the rare bleeding disorder.
Queen Victoria's descendants with haemophilia and known female carriers Inheritance by female carriers. Haemophilia figured prominently in the history of European royalty in the 19th and 20th centuries.
Baxter to Initiate Late-Stage Clinical Trial of BAX 855 for the Treatment of Hemophilia A Company Announces Top-line Phase I Clinical Data DEERFIELD, Ill.--(BUSINESS WIRE)-- Baxter International ...
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