Presentation Information
[O30-03]A Case of Angelman syndrome with 15q11q13 deletion, challenging to clinically differentiate from Prader-Willi syndrome
○Ryoji Taira1, Kentaro Marutani1, Yuji Ueno1, Saori Kawakami1, Kousuke Yonemoto1, Michiko Torio1, Takeshi Kusuda2, Ryutaro Kira1 (1.Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan, 2.Department of Neonatology, Fukuoka Children's Hospital, Fukuoka, Japan)