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Giansily-Blaizot, M., Verdier, R., Biron-Adréani, C., Schved, J.F., Bertrand, M.A., Borg, J.Y., et al. (2004) Analysis of Biological Phenotypes from 42 Patients with Inherited Factor VII Deficiency: Can Biological Tests Predict the Bleeding Risk? Haematologica, 89, 704-709.

has been cited by the following article:

• TITLE: Factor VII Deficiency: A Rare Cause of Severe Bleeding Disorder in a Newborn

  AUTHORS: Hanane Hajaj, Hanae Bahari, Anass Ayyad, Sahar Messaoudi, Rim Amrani

  KEYWORDS: Congenital Deficiency, Factor VII, Hemorrhage

  JOURNAL NAME: Open Journal of Pediatrics, Vol.13 No.6, November 14, 2023

  ABSTRACT: Factor VII deficiency is rare. It is an autosomal recessive inherited disease with an estimated prevalence of 1/1,000,000. We report the case of a newborn male from first-degree consanguineous parents admitted at 15 days of life due to a hemorrhagic syndrome. Hemostasis tests showed low prothrombin time (PT) and normal activated partial thromboplastin time (aPTT). A coagulation panel revealed isolated factor VII deficiency. In this case, we highlight the clinical, biological, and therapeutic aspects of this condition during the neonatal period.