Presentation Information
[P1-01-14]A case of Kallmann syndrome diagnosed by a novel FGFR1 gene mutation and had a live birth after long-term management
○Itsuki Kajimura1, Shoko Miura1, Sayaka Kawashita1, Riko Matsuda3, Yuriko Kitajima1, Yuri Hasegawa1, Hiroyuki Mishima2, Akira Kinoshita2, Koh-ichiro Yoshiura2, Kiyonori Miura1 (1.Department of Obstetrics and Gynecology, Nagasaki University Hospital, Nagasaki, Japan, 2.Department of human genetics, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, 3.Clinical Genomics Center, Nagasaki University Hospital)