Hemophilia in the newborn without family history--pattern of clinical presentation of three patients

• Published in: Vojnosanitetski pregled Vol. 67; no. 10; pp. 861 - 863
• Main Authors: Kuzmanovic, Milos, Jankovic, Borisav, Rasovic-Gvozdenovic, Nada, Martic, Jelena, Serbic, Olivera
• Format: Journal Article
• Language: English
• Published: Serbia Military Health Department, Ministry of Defance, Serbia 01-10-2010
• Subjects: Cerebral Hemorrhage - diagnosis; Cerebral Hemorrhage - etiology; diagnosis, differential; factor VIII; Hematoma - diagnosis; Hematoma - etiology; hemophilia A; Hemophilia A - complications; Hemophilia A - diagnosis; Humans; Infant, Newborn; Male; neonatology
• ISSN: 0042-8450; 2406-0720
• DOI: 10.2298/VSP1010861K

Hemophilia is the most frequently diagnosed inborn clotting factor deficiency in the newborn. In about half of the cases diagnosis is made during neonatal period. However, due to different clinical presentation comparing to older children, hemophilia in the newborn could be misdiagnosed, especially in the setting of negative family history.
Clinical features of three newborns with negative family history for hemophilia are described. All three newborns were the first born children with uneventful perinatal history, and they were referred for investigation of convulsions, soft tissue tumorous mass and sepsis, respectively. Prompt diagnosis of underlying bleeding disorder and adequate substitution therapy lead to the good outcome in all three boys.
Symptoms and signs of hemophilia in the newborn could be at time misleading and contribute to delayed treatment. High index of suspicion on inherited bleeding disorder is warranted in every neonate with intracranial bleeding.