Napolitano, M., Siragusa, S. and Mariani, G. (2017) Factor VII Deficiency: Clinical Phenotype, Genotype and Therapy. Journal of Clinical Medicine, 6, 38.
https://doi.org/10.3390/jcm6040038

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.