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[O7-2]Exploring Unsolved Cases of Lissencephaly Spectrum: Integrating Exome and Genome Sequencing for Higher Diagnostic Yield
○Shogo Furukawa1, Mitsuhiro Kato2, Akihiko Ishiyama3, Tomohiro Kumada4, Takeshi Yoshida5, Eri Takeshita3, Pin Fee Chong6, Hideo Yamanouchi7, Kazuo Abe8, Yuko Kotake9, Takayoshi Kyoda10, Toshihiro Nomura11, Miyata Yohane12, Mitsuko Nakashima1, Hirotomo Saitsu1 (1.Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan, 2.Department of Pediatrics, Showa University School of Medicine, 3.Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry, 4.Kumada kids-family clinic, 5.Department of Pediatrics, Kyoto University Graduate School of Medicine, 6.Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, 7.Department of Pediatrics, Saitama Medical University, Saitama, Japan, 8.Division of Neurology, Hyogo College of Medicine College Hospital, Nishinomiya, Japan, 9.Department of Pediatrics, The Jikei University School of Medicine, Tokyo, Japan, 10.Children's Medical Center, Showa University Northern Yokohama Hospital, Yokohama, Japan, 11.Department of Pediatrics, Kawaguchi Municipal Medical Center, Saitama, Japan, 12.Department of Pediatrics, Kyorin University School of Medicine, Tokyo, Japan)