BAYRAKTAR, BilgeBayraktar, SuleymanARSLAN, HÜSEYİNÇAKIR, FATMA BETÜL2020-10-222020-10-222016-12-01BAYRAKTAR B., Bayraktar S., ARSLAN H., ÇAKIR F. B. , -Freeman-Sheldon Syndrome Associated with Hemophilia-A in a Newborn-, HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI, cilt.54, ss.243-245, 2016http://hdl.handle.net/20.500.12645/24172The Freeman-Sheldon syndrome (FSS) (whistling face) is a congenital autosomal dominant disease (rarely described in its autosomal recessive form) characterized by small -whistling- mouth, a flat masklike face, joint contractures (commonly involving the fingers and hands) and underdevelopment of the nasal cartilage. Other clinical features include full forehead, deep set eyes, epicanthal folds, high palate, H-shaped cutaneous dimpling on the chin, ulnar deviation of the hands, seizures, and dislocation of the hip. A 10-day-old male newborn was admitted to our neonatal intensive care unit with jaundice and hyperthermia. He had fever of 42.5 degrees C, small whistling mouth, a flat mask-like face, joint contractures of the fingers, and ulnar deviation of the hands. The parents were consanguineous and one of the boys died when he was 1 years old due to intracranial hemorrhage. To our knowledge, there have been more than 60 cases diagnosed with FSS. This is the first reported case of Freeman-Sheldon syndrome associated with hemophilia A and the second case of FSS associated with fever without anesthesia.ArticleWOS:0003912000000108500849735310.4274/haseki.2915trdizin