Inherited coagulation disorders in newborns in the early neonatal period

Abstract

The article presents a rare case of a hereditary coagulation disorder (factor VIII deficiency). Тhe reported rare case of hemophilia A manifestation in a child in the early neonatal period emphasizes the need for an accurate collection of a family history of bleeding, as well as an assessment of specific clinical and laboratory data and a differential diagnosis with other disorders of the blood coagulation system. The clinical manifestations of hemorrhagic syndrome were not specific; they allowed us to determine the direction of the laboratory search for violations of primary and secondary hemostasis. Clarification of the diagnosis and the choice of gemostatic therapy were performed after a laboratory study of blood coagulation. The presented studies reflect the most typical errors at the stages of diagnosis and correction of blood coagulation disorders, which will improve the quality of medical care for newborns in the future.