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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
Review Open access 2026

A Rare Case of Adult-Onset Acute Disseminated Encephalomyelitis Presenting with Seizure and Acute Confusion: A Case Report and Literature Review

Acute disseminated encephalomyelitis (ADEM) is an immune-mediated inflammatory demyelinating disorder of the central nervous system, typically encountered in the pediatric population. Adult-onset ADEM is uncommon and poses a diagnostic challenge, particularly when presenting with seizure as a cardinal feature and when...

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

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