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    • Subarachnoid hemorrhage in congenital factor X deficiency: A case study and literature review 

      Sepideh Mohammadi; Zahra Torab; Soheila Aghakhani; Mina Ghalandari; Reyhaneh Mohammadimanesh; Vahid Asgary; Samira Louni Aligoudarzi; Mohammad Reza Younesi (2016-12-01)
      © 2016, Iranian Red Crescent Medical Journal. Background: Inborn factor X deficiency (FXD) is a very rare (1: 500,000) hereditary coagulation disorder, which is characterized by clinical manifestations including hematoma, ...