The 66th Annual Meeting of the Japanese Society of Child Neurology

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General Oral Presentation

[O31] 遺伝・先天異常 3

Sat. Jun 1, 2024 10:50 AM - 11:50 AM Room8 (Bldg.1 3F 131＋132)

Organizer:Kenji Shimizu(Division of Clinical Genetics and Cytogenetics, Shizuoka Children's Hospital),Iori Ohmori(Institute of Academia and Research, Okayama University)

[O31-2] A girl case with L1 syndrome that may have developed due to skewed X inactivation.

○Tatsuo Mori1, Mutsuki Nakano1, Takahiro Tayama1, Aya Goji1, Yoshihiro Toda1, Shinichi Kameyama2, Takeshi Mizuguchi2, Naomichi Matsumoto2, Maki Urushihara1 (1.Department of Pediatrics, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japa, 2.Department of Human Genetics, Yokohama City University, Graduate School of Medicine, Yokohama, Japan)

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