The 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society / The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology

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APPES/JSPE Joint Session(English)

APPES/JSPE Joint Session(English) » Tea Break&Poster Discussion

P2-8: Bone & minerals

Sat. Nov 19, 2016 3:10 PM - 4:00 PM Poster & Exhibition Room (Hall B5)

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

○Noboru Uchida1,2, Reiko Horikawa1 (1.Division of Endocrinology and Metabolism, National Center for Child Health and Development, 2.Department of Pediatrics, Saiseikai Utsunomiya Hospital)

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