[P1] 遺伝・先天異常

[P1-33] A case of Prader-Willi syndrome with accelerated development in infancy by Coenzyme Q10

^○Konomi Shimoda^1,2, Hiroshi Terashima¹, Yu Kakimoto¹, Shunpei Uchino¹, Kei Murayama³ (1.Department of Pediatrics, University of Tokyo,Tokyo,Japan, 2.Department of Pediatrics, National Rehabilitation Center for Children with Disabilities, Tokyo, Japan, 3.Diagnostics and Therapeutics of Intractable Disease, Intractable Disease Research Center,Juntendo University Faculty of Medicine)