Myelination disturbance in a patient with hyperuricemia and hyperserotoninemia combined with 18Q deletion syndrome

Aranka LASZLO1, Erika VOROS2, Klara BUGA3, Katalin HORVATH4, Peter MAYER5, †Magda OSZTOVICS6, Laszlo PAVICS7, Andras SVEKUS8, Marc C. PATTERSON9 1Department of Pediatrics and Children's Health Center, Albert Szent-Gyorgyi Medical Centre, University of Szeged, Szeged 2Department of Radiology, Albert Szent-Gyorgyi Medical Centre, University of Szeged, Szeged 3Clinic of Nuclear Medicine, Imre Haynal Health Science University, Budapest 4Department of Radiology, Imre Haynal Health Science University, Budapest 5Department of Neurology Erzsebet Hospital, Hodmezovasarhely 6Department of Genetics, Agost-Schopf-Merei Hospital, Budapest 7Department of Nuclear Medicine, Albert Szent-Gyorgyi Medical Centre, University of Szeged, Szeged 8Kalman Pandy Hospital, Department of Paediatrics, Gyula 9Division of Pediatric Neurology, Departments of Neurology and Pediatrics, Columbia University, New York