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Iranian Journal of Medical Sciences، جلد ۳۲، شماره ۳، صفحات ۱۳۱-۰
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عنوان انگلیسی Combined Factor V and VIII Deficiency
چکیده انگلیسی مقاله This review summarizes current data on the pathomechanisms and new genetic findings of combined factor V and VIII deficiency (CF5F8D). Congenital haemorrhagic disorders characterized by deficiency of two clotting factors comprise an interesting group. Among dual coagulation disorders, CF5F8D is the most common type. For the first time combined factor V and VIII deficiency (F5F8D) was reported by Oeri et al in 1954. That is distinct from the coinheritance of both FV deficiency (parahaemophilia) and FVIII deficiency (haemophilia A) that has been reported in four families . Individuals who present with this phenotype have between 5 and 30% of normal plasma levels of FV and FVIII antigen and activity, whereas the level of other plasma proteins are not altered . Total numbers of affected individuals are less than 150 cases in all over the world. At first it was assumed that deficiency of protein C inhibitor was a responsible cause, but further investigations revealed that it was due to mutations called ERGIC-53 and LMAN-1.
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نویسندگان مقاله حسن منصوری طرقبه | hassan mansouritorghabeh


نشانی اینترنتی http://ijms.sums.ac.ir/index.php/IJMS/article/view/1857
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زبان مقاله منتشر شده en
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نوع مقاله منتشر شده Review Article
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