British Journal of Haematology · 1998 · 105 citations · 7 references
MedicineHematologyHematopathologyHemostasisHuman GeneticsBleeding DisordersCoagulation AbnormalitiesCoagulation DisordersCoagulation Factor DeficienciesCoagulation PhysiologyHemostatic DisordersBleedingBleeding ManifestationsClinical Manifestations In AdultsCoagulationCombined Coagulation DefectsFactor Viii AlterationsHereditary Factor V DeficiencyInherited Coagulation Factor Deficiencies
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.
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Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency
Flora Peyvandi, P.M. Mannucci, Daniela Asti et al. · Haemophilia · 1997 · 100 citations
Medicine, Hematology, Surgery +15
Heterogeneity of von Willebrand's disease: Study of 40 Iranian Cases
Irandokht Shoa'i, J. M. Lavergne, N Ardaillou et al. · British Journal of Haematology · 1977 · 53 citations
Medicine, Hematology, Pathology +17