Peyvandi F, Tuddenham E G, Akhtari A M, Lak M, Mannucci P M
Haemophilia Centre, Iman Khomeini Hospital, Tehran, Iran.
Br J Haematol. 1998 Mar;100(4):773-6. doi: 10.1046/j.1365-2141.1998.00620.x.
Inherited deficiency of factors V and VIII is the most frequent combined coagulation defect. The cases reported so fair are mostly single cases or small series from different centres, making it difficult to evaluate the overall pattern of clinical manifestations of the combined defect. We examined at a single institution 27 Iranian patients. Mucocutaneous and post-surgical bleeding were the most frequent clinical manifestations. The presence of two defects did not make the severity of bleeding greater than that expected in patients with single coagulation defects of similar degrees.
