P1-7: Adrenals

[P1-7-1] Mortality and incidence of misidentification of sex assignment in patients with congenital 21-hydroxylase deficiency identified by a newborn screening program in Japan (2001-2015).

^○Takasawa Kei^1,2, Ishii Tomohiro^2,3, Okada Satoshi^2,4, Kamasaki Hotaka^2,5, Kubota Takuo^2,6, Kobayashi Hironori^2,7, Sawada Hirotake^2,8, Nagasaki Keisuke^2,9, Numakura Chikahiko^2,10, Harada Shohei^2,11, Minamitani Kanshi^2,12, Sugihara Shigetaka^2,13, Adachi Masanori^2,14, Tajima Toshihiro^2,15 (1.Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, 2.the Committee for the newborn screening, the Japanese Society for Pediatric Endocrinology, 3.Department of Pediatrics, Keio University School of Medicine, 4.Department of Pediatrics, Hiroshima University Graduate School of Biomedical & Health Sciences, 5.Department of Pediatrics, Sapporo Medical University School of Medicine, 6.Department of Pediatrics, Osaka University Graduate School of Medicine, 7.Department of Pediatrics, Shimane University School of Medicine, 8.Division of Pediatrics, University of Miyazaki Faculty of Medicine, 9.Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medical and Dental Sciences, 10.Department of Pediatrics, Yamagata University School of Medicine, 11.Division of Neonatal Screening, National Center for Child Health and Development, 12.Department of Pediatrics, Teikyo University Chiba Medical Center, 13.Department of Pediatrics, Tokyo Women's Medical University Medical Center East, 14.Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, 15.Pediatrics, Jichi Children's Medical Center Tochigi)