Trombocitopenia por heparina desordenes del grupo 2. Factor v deficiency is usually caused by mutations in the f5 gene, which provides instructions for making a protein called coagulation factor v. Factor xi deficiency is a hereditary coagulation disorder with a quantitative andor qualitative reduc. Pdf deficiencia congenita del factor v researchgate.
Technical manual, american association of blood banks, 12. As a result, people affected by this condition may have difficulty stopping the flow of blood following dental extractions, trauma or surgery. Factor xi deficiency genetic and rare diseases information. Presentan hemorragias moderadas, y hemorragias graves. Deficit en facteur xii deficit congenital en facteur hageman deficit congenital en facteur xii.
Deficiencia congenita del factor v scielo colombia. A b c d e f g h i j k l m n o p q r s t u v w x y z az listings contact us. Deficiencia congenita del factor v congenital deficiency of factor v hernan dario aguirreh 1 andres felipe posadal, jorge enrique aponte. Diagnostico al laboratorio actividad del factor x baja. Factor xi deficiency is a bleeding disorder that interferes with the bodys clotting process. Hemorragia, razon normalizada internacional, deficiencia factor v. F5 gene mutations that cause factor v deficiency prevent the production of functional coagulation. Renelevesque ouest bureau 1200 montreal, quebec h3g 1t7 canada telefono. Clinical and laboratory standards institute document h4a6. Spanish multimedia encyclopedia deficiencia del factor vii. Feb 05, 2016 factor xi deficiency is a bleeding disorder that interferes with the bodys clotting process. This protein plays a critical role in the coagulation system, which is a series of chemical reactions that forms blood clots in response to injury. Deficiency, factor xii deficiencies, factor xii factor xii deficiencies trait, hageman.
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