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-101] A case of siblings with early infantile epilepsy due to hemiplegic PRRT2 gene mutation.

○Hikari Kaba1, Saoko Takeshita1, Yoshihiro Watanabe1, Hirotaka Motoi1, Yu Fujiwara1, Naomichi Matsumoto2, Mitsuko Nakashima2 (1.Department of Pediatrics, Yokohama City University Medical Center, Yokohama, Japan, 2.Department of Human Genetics, Yokohama City University Graduate School of Medecine, Yokohama, Japan)

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