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What is the clinical deficiency presented by hemophilic people? What is the genetic cause of that deficiency?
The Hemophilia is a disease characterized by impaired blood clotting and the affected person is more prone to internal and external hemorrhages.
The Patients with hemophilia A have alteration in the gene that codifies the factor VIII of blood clotting a gene located in the non-homologous portion of the X chromosome. The Patients with hemophilia B present a defect of the gene that codifies the factor IX of clotting, a gene also located in the non- homologous region of the X chromosome. Therefore both diseases are X- linked diseases.
phases of alpha taxonomy
Blood transfusion The blood of Raja cannot be transfused to Rama because the blood group of Raja is ‘B' and blood group of Rama is ‘A'. If Raja's blood with group ‘B' is
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