[P2-07] Poster Session 2-07　Rare Diseases 2

[P2-07-17] National interview survey for patients with Hutchinson-Gilford syndrome and progeroid laminopathies and their families

Yuko Okawa¹, Nobue Tsukatani², Masanori Inoue^1,2, Muneaki Matsuo³, Rika Kosaki⁴, Kenichi Kashimada⁵, Keiichi Ozono^6,7, Hiroyuki Saitou⁷, Tatsuya Nakamichi⁷, Masanobu Fujimoto⁸, Noriyuki Namba⁸, Hidefumi Tonoki⁹, Yuko Murai¹⁰, Kenji Ihara^1,2 (1.Department of Pediatrics, Faculty of Medicine, Oita University, Oita, Japan, 2.Genetic Medical Center, Oita University Hospital, Oita, Japan, 3.Department of Pediatrics, Faculty of Medicine, Saga University, Saga, Japan, 4.Division of Medical Genetics, National Center for Child Health and Development, Tokyo, Japan, 5.Division of Endocrinology and Metabolism, National Center for Child Health and Development, Tokyo, Japan, 6.Center for Promoting Treatment of Intractable Diseases, Iseikai International General Hospital, Osaka, Japan, 7.Department of Pediatrics, Iseikai International General Hospital, Osaka, Japan, 8.Division of Pediatrics and Perinatology, Faculty of Medicine, Tottori University, Tottori, Japan, 9.Medical Genetics Center, Department of Pediatrics, Tenshi Hospital, Hokkaido, Japan, 10.Department of Pediatrics, Yaeyama Hospital, Okinawa, Japan)

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