Session Details
[OE7]Oral English Session 7 Cardiovascular Disorders
Sat. Oct 12, 2024 9:00 AM - 9:50 AM JST
Sat. Oct 12, 2024 12:00 AM - 12:50 AM UTC
Sat. Oct 12, 2024 12:00 AM - 12:50 AM UTC
Room 5(Highness Hall, 2F)
Chairs:Hiroko Morisaki(Sakakibara Heart Institute), Yoshihiro Asano(National Cerebral and Cardiovascular Center・Osaka University)
[OE7-1]Identifying variants with moderate effect size on familial hypercholesterolemia
○Pei-Chieng Cha1, Mika Hori2, Mariko Harada-Shiba3, Atsushi Takahashi1 (1.Department of Genomic Medicine, Research Institute, National Cerebral and Cardiovascular Center (NCVC), 2.Department of Endocrinology, Research Institute of Environmental Medicine, Nagoya University, 3.Cardiovascular Center, Osaka Medical and Pharmaceutical University)
[OE7-2]The RNF213 p.R4810K Variant: A Key Risk for East Asian Cerebral and Cardiovascular Disease
○Hiroyuki Ishiyama1, Takeshi Yoshimoto1, Atsushi Takahashi2, Soichiro Abe1, Ryoma Inui1, Yoshihiro Asano3, Masafumi Ihara1 (1.Department of Neurology, National Cerebral and Cardiovascular Center, 2.Department of Genomic Medicine, National Cerebral and Cardiovascular Center, 3.NCVC Biobank, National Cerebral and Cardiovascular Center)
[OE7-3]Inherited heart disease of sudden unexpected death in young revealed by post-mortem genetic testing: systematic review
○Kanako Koike Fukushima1,2, Takahiro Itaya3, Yuko Kamiakito1, Masakazu Nishigaki1,2, Seiko Ohno4, Hirokazu Kotani5, Shoji Tsuji2,6 (1.Depart of Genetic Counseling, International University of Health and Welfare Graduate School, Tokyo, Japan, 2.International University of Health and Welfare Narita Hospital, Chiba, Japan, 3.Department of Healthcare Epidemiology, Graduate School of Medicine and Public Health, Kyoto University, Kyoto, Japan, 4.Medical Genome Center, National Cerebral and Cardiovascular Center, Osaka, Japan, 5.Department of Forensic Medicine and Sciences, Mie University Graduate School of Medicine, Mie, Japan, 6.Institute of Medical Genomics, International University of Health and Welfare, Chiba, Japan)
[OE7-4]Identification of PTGIS Variants in Patients with Williams Syndrome and Severe Peripheral Pulmonary Stenosis
○Ayako Nagai1,2, Hiroyuki Akagawa3, Saori Sawai1, Tatsuya Kato4, Satoshi Yakuwa5, Jun Muneuchi6, Kazushi Yasuda7, Hirokuni Yamazawa1, Toshiyuki Yamamoto8, Emi Takakuwa9, Utano Tomaru9, Yoshiyuki Furutani2, Harada Gen2, Kei Inai2, Toshio Nakanishi2, Atsushi Manabe1, Atsuhito Takeda1 (1.Department of Pediatrics, Hokkaido University, Sapporo, Japan, 2.Department of Pediatric Cardiology and Adult Congenital Cardiology, Tokyo Women's Medical University, Tokyo, Japan, 3.Institute for Comprehensive Medical Sciences, Tokyo Women's Medical University, Tokyo, Japan, 4.Department of Thoracic Surgery, Hokkaido University Hospital, Sapporo, Japan, 5.Department of Pediatrics, Obihiro Kosei Hospital, Obihiro, Japan, 6.Department of Pediatrics, Kyushu Hospital Japan Community Healthcare Organization, Kitakyusyu, Japan, 7.Department of Pediatric Cardiology, Aichi Children's Health and Medical Center, Obu, Japan, 8.Division of Gene Medicine, Graduate School of Medical Science, Tokyo Women's Medical University, Tokyo, Japan, 9.Department of Surgical Pathology, Hokkaido University Hospital, Sapporo, Japan)
[OE7-5]Unexpected Genetic Findings in Hereditary Connective Tissue Disease Associated with Annuloaortic Ectasia
○Hidenori Yamamoto1,2, Ayako Tanabe3, Mami Morita4, Maki Morikawa4, Miki Hatakeyama4, Kentaro Suzuki1, Yoshihito Morimoto1, Kiyotaka Go1, Yoshie Fukasawa1, Naoki Ohashi1, Taichi Kato1 (1.Childrens Heart Center, Nagoya University Hospital, 2.Department of Pediatrics, TOYOTA Memorial Hospital, 3.Department of Medical Genetics, TOYOTA Memorial Hospital, 4.Center for Medical Genetics, Nagoya University Hospital)