[O8] Oral Presentation
teratology　2

[O-046] Mutations in MAGEL2 cause a novel imprinting disorder distinct from Prader-Willi syndrome

^○Yutaka Negishi¹, Daisuke Ieda¹, Ikumi Hori¹, Ayako Hattori¹, Yasuyuki Nozaki², Hirofumi Komaki³, Jun Tohyama⁴, Keisuke Nagasaki⁵, Hiroko Tada⁶, Hiroshi Masaki⁷, Shinji Saitoh¹ (1.Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan, 2.Department of Pediatrics, Jichi Medical University , Tochigi, Japan, 3.Department of Child Neurology , National Center Hospital, National Center of Neurology and Psychiatry (NCNP) , Tokyo , Japan, 4.Department of Child Neurology Nishi-Niigata Chuo National Hospital Niigata, Japan, 5.Division of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan, 6.Department of Pediatrics, Chibaken Saiseikai Narashino Hospital, Narashino, Japan, 7.Department of Pediatrics and Neonatology, St. Marianna University Yokohama-City Seibu Hospital, Yokohama, Japan)