Jovandaric, Miljana Zivojin (56748058300)Miljana Zivojin (56748058300)JovandaricJesic, Milos M. (57211511149)Milos M. (57211511149)Jesic2025-06-122025-06-122015https://doi.org/10.3109/15513815.2015.1051250https://www.scopus.com/inward/record.uri?eid=2-s2.0-84938379237&doi=10.3109%2f15513815.2015.1051250&partnerID=40&md5=4a70118aef670814a5bec7e6c39c65e9https://remedy.med.bg.ac.rs/handle/123456789/8096Hemophilia is the most common inherited coagulation disorder, and approximately one-half of patients are diagnosed as newborns. For prenatal diagnosis of hemophilia A, genetic tests are performed using chorionic villi (biopsy PCR chorionic villi sampling [CVS]) at 10 weeks' of gestation. The result in this fetus demonstrated an inversion within intron 1 in part for hemophilia A. This male infant, who was his parents' first offspring, was born after an uneventful pregnancy. An uncle suffered from hemophilia A. This report describes a newborn who was prenatally diagnosed with hemophilia A. The timely diagnosis of hemophilia in a newborn enabled the provision of adequate therapy, which led to a favorable outcome. © 2015 Informa Healthcare USA, Inc.coagulation disorderhemophilia Anewborn