Ppt Hemophilia Powerpoint Presentation Free Download Id 6176299 Presentation transcript. genetic cause • hemophilia is a recessive sex linked disorder. • the mutated gene that accounts for hemophilia is located on the x chromosome. • a mutation in the f8 gene causes hemophilia a, and a mutation in the f9 gene causes hemophilia b. • these mutations result in an absence of several proteins required. In 1960, fxiii deficiency was described. a royal disease hemophilia is sometimes referred to as “the royal disease,” because it affected the royal families of england, germany, russia and spain in the 19th and 20th centuries. queen victoria of england, who ruled from 1837 1901, is believed to have been the carrier of hemophilia b, or factor.
Ppt Hemophilia Powerpoint Presentation Free Download Id 6176299 Hemophilia chronic genetic disorder characterized by a protein deficiency that results in delayed blood clotting. individuals with hemophilia typically have internal bleeds affecting their joints and muscles. while hemophilia is the result of a mutation on the x chromosome, approximately 33% of cases are random mutations and not inherited. About this presentation. description : check out this medical powerpoint presentation titled "hemophilia”. this medical powerpoint presentation is about hemophilia, a rare genetic disorder that affects the bloods ability to clot properly. people with hemophilia have a deficiency in one of the clotting factors, which are proteins that work. Hemophilia. hemophilia is a rare bleeding disorder caused by missing or defective clotting factors, resulting in an inability to form blood clots. there are three main types: hemophilia a caused by factor viii deficiency, hemophilia b caused by factor ix deficiency, and acquired hemophilia which is autoimmune in nature. symptoms include. Hemophilia: history, overview, and treatment •review human hemostasis. •discuss hemostatic defects present in hemophilia and the symptoms caused. •discuss treatments for hemophilia patients. objectives •hereditary bleeding disorders •deficiencies or defects in proteins involved in blood clotting coagulation.
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