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

Presentation information

Print

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-100] Two siblings case of paroxysmal kinesigenic dyskinesia with a novel truncation mutation of PRRT2

○Makoto Kita1, Yasuhiro Kwata2, Nagako Murase2, Yuichi Akiyama1, Takeshi Usui3 (1.National Hospital Organization Kyoto Medical Center, Department of Pediatrics, Kyoto, Japan, 2.National Hospital Organization Kyoto Medical Center, Department of Neurology, Kyoto, Japan, 3.Shizuoka General Hospital, Department of Medical Genetics, Shzuoka, Japan)

Abstract password authentication.
Password is required to view the abstract. Please enter a password to authenticate.

Password