The 59th Annual Meeting of the Japanese Society of Child Neurology

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Oral Presentation

genetic abnormality

[O17] Oral Presentation
teratology 3 -case report-

Fri. Jun 16, 2017 4:20 PM - 5:30 PM Room No.6 (10F Conference Room 1009)

Chair:Shinji Saitoh(Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan), Shinsuke Ninomiya(Department of Clinical Genetics, Kurashiki Central Hospital, Okayama, Japan)

[O-099] A case of FOXG1 gene deletion with postnatal microcephaly, epilepsy and movement disorder

○Wakaba Endo, Yusuke Takezawa, Yukimune Okubo, Takehiko Inui, Sato Suzuki, Takuya Miyabayashi, Noriko Togashi, Kazuhiro Haginoya (Miyagi Children's Hospital, Sendai, Japan)

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