[P1-08] Poster Session 1-08　Rare Diseases 1

[P1-08-2] A Rare Case of Kartagener Syndrome with Situs Inversus and Homozygous Exon 1-4 Deletion in DRC1

Junko Miyamoto¹, Tetsuya Okazaki^2,9, Saki Shinzato^3,9, Tomoki Nonaka^4,9, Kohei Watanabe⁵, Koshi Kawakami^6,9, Naoki Yoshino⁷, Akiyoshi Kanazawa^8,9 (1.Department of Obstetrics and Gynecology, Shimane Prefectural Central Hospital, Shimane, Japan, 2.Department of Clinical Genomic Medicine, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan, 3.Division of Medical Education, Faculty of Medicine, Tottori University, Tottori, Japan, 4.Department of Clinical Genetics, Tottori University Hospital, Tottori, Japan, 5.Department of Respiratory Medicine, Shimane Prefectural Central Hospital, Shimane, Japan, 6.Department of Clinical Oncology, Shimane Prefectural Central Hospital, Shimane, Japan, 7.Department of Gynecology, Tokushukai Medical Corporation Izumo Tokushukai, Shimane, Japan, 8.Department of Gastroenterological Surgery, Shimane Prefectural Central Hospital, Shimane, Japan, 9.Clinical Genomic Medicine Promotion Office, Shimane Prefectural Central Hospital, Shimane, Japan)

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