P2-8: Bone & minerals

[P2-8-10] An effective case of enzyme replacement therapy for perinatal hypophosphatasia with a novel mutation in ALPL gene.

^○Maki Oyachi¹, Daisuke Harada¹, Yuki Hanioka¹, Natsuko Sakamoto¹, Kaoru Ueyama¹, Kawai Kondo¹, Kanako Kishimoto¹, Masafumi Izui¹, Yuiko Nagamatsu¹, Hiroko Kashiwagi¹, Miho Yamamuro¹, Yoshihito Ishiura¹, Makoto Tamura², Shin Kikuchi², Tomoyuki Akiyama³ (1.Department of Pediatrics, Japan Community Health care Organization（JCHO）Osaka Hospital, 2.Department of Pediatrics and Neonatology, Takatsuki General Hospital, Takatsuki, 3.Department of Child Neurology, Okayama University Graduate School of Medicine and Dentistry, 4.Department of Bone and Mineral Research, Osaka Medical Center and Research Institute for Maternal and Child Health)