%0 Journal Article %T Factor VII Deficiency: A Rare Cause of Severe Bleeding Disorder in a Newborn %A Hanane Hajaj %A Hanae Bahari %A Anass Ayyad %A Sahar Messaoudi %A Rim Amrani %J Open Journal of Pediatrics %P 894-899 %@ 2160-8776 %D 2023 %I Scientific Research Publishing %R 10.4236/ojped.2023.136097 %X 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. %K Congenital Deficiency %K Factor VII %K Hemorrhage %U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=129006