Oral 3: Pituitary & Others (CCS, dyslipidemia, etc)

Fri. Nov 18, 2016 10:45 AM - 11:45 AM Room 3 (Hall B7 (2))

Moderator: Koji Muroya (Depertment of Endocrinology and Metabolism, Kanagawa Children's Medical Center), Louis Low (Department of Paediatrics Hong Kong Sanatorium and Hospital Hong Kong)

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10:45 AM - 10:55 AM

[O3-1] Analysis of endocrinopathy as late effects in Childhood cancer survivors at a single institute in Japan

^○Tomoko Yoshida¹, Kanako Nakao¹, Yuta Chiba¹, Yumiko Terada¹, Yasuko Ogiwara¹, Keisuke Yoshii¹, Chikako Kiyotani^1,2, Yoko Shioda², Tomoo Osumi², Daisuke Tomizawa², Motohiro Kato², Kimikazu Matsumoto², Yasuhiro Naiki¹, Reiko Horikawa¹ (1.Division of Endocrinology and Metabolism, National Center for Child Health and Development, 2.Children's Cancer Center, National Center for Child Health and Development)

10:55 AM - 11:05 AM

[O3-2] Genome-wide analysis of differential DNA methylation in Silver-Russell syndrome

^○Di Wu, Chunxiu Gong (Department of Endocrinology, Genetics and Metabolism, Beijing Children’s Hospital, Capital Medical University)

11:05 AM - 11:15 AM

[O3-3] Serum antim?llerian hormone and inhibin B as potential markers for progressive central precocious puberty in girls

^○Linqi Chen, Ting Chen, Haiying Wu, Fengyun Wang, Xiuli Chen, Rongrong Xie (Division of Endocrinology and Metabolism / Department of Pediatrics, The Children's Hospital of Soochow University)

11:15 AM - 11:25 AM

[O3-4] Genotype and phenotype of 101 Vietnamese Patients with Congenital Hyperinsulinism

^○Dung Vu¹, Duong Dang¹, Ngoc Can¹, Khanh Nguyen¹, Thao Bui¹, Hai Le¹, Dat Nguyen¹, Dien Tran¹, Ellard Sian², Flanagan Sarah² (1.Department of Endocrinology, Metabolism and Genetics, National Children's Hospital. Hanoi, Vietnam, 2.Molecular Genetics, Royal Devon & Exeter NHS, University of Exeter Medical School. UK)

11:25 AM - 11:35 AM

[O3-5] Short and long-term outcome of patients with congenital hyperinsulinism

^○Yumiko Terada, Yusuke Fujisawa, Yuta Chiba, Yasuko Ogiwara, Tomoko Yoshida, Kanako Nakao, Keisuke Yoshii, Yasuhiro Naiki, Reiko Horikawa (Division of Endocrinology and Metabolism, National Center for Child Health and Development)

11:35 AM - 11:45 AM

[O3-6] Rare frequency of mutations in pituitary transcription factor genes in patients with combined pituitary hormone deficiency or isolated growth hormone deficiency in Korea

^○Yoon-Myung Kim Kim¹, Eungu Kang¹, Jin-Ho Choi¹, Chang-Woo Jung¹, Sun Hee Heo², Minji Kang², Gu-Hwan Kim³, Beom Hee Lee¹, Han-Wook Yoo¹ (1.Department of Pediatrics,, Asan Medical Center Children’s Hospital, University of Ulsan College of Medicine, Seoul, Korea, 2.Asan Institute for Life Sciences, Asan Medical Center Children’s Hospital, University of Ulsan College of Medicine, Seoul, Korea, 3.Medical Genetics Center, Asan Medical Center Children’s Hospital, University of Ulsan College of Medicine, Seoul, Korea)