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Mohammed Alkahtib

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Open access 2026

Isolated Severe Prolongation of Prothrombin Time Revealing Congenital Factor VII Deficiency With Mild Bleeding Phenotype: A Case Report

Congenital Factor VII (FVII) deficiency is a rare inherited bleeding disorder characterized by marked variability in bleeding severity and poor correlation between factor activity levels and clinical phenotype. We report a 21-year-old woman who presented with recurrent spontaneous ecchymoses without mucosal bleeding, m...

Mohammed Alkhanafsa, O. Mosleh, Jamil Wafi et al. · 0 citations

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