[P1] 遺伝・先天異常

[P1-39] A case of MECP2 duplication syndrome diagnosed by array CGH and required genetic counseling.

^○Naoya Higuchi¹, Takuji Nakamura¹, Masafumi Sanefuji¹, Tomoko Yamamoto², Hidenobu Soejima³, Toshiyuki Yamamoto⁴, Muneaki Matsuo¹ (1.Department of Pediatrics,University of Saga,Saga,Japan, 2.Department of Obstetrics and gynecology,University of Saga,Saga,Japan, 3.Division of Molecular Genetics and Epigenetics, Department of Biomolecular Sciences, Faculty of Medicine, Saga University, Saga,Japan, 4.Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan.)