P2-8: Bone & minerals

[P2-8-1] A case with acrodysostosis and familial exudative vitreoretinopathy having p.R368X mutation in PRKAR1A gene

^○Noboru Uchida^1,2, Reiko Horikawa¹ (1.Division of Endocrinology and Metabolism, National Center for Child Health and Development, 2.Department of Pediatrics, Saiseikai Utsunomiya Hospital)