A case of infantile epileptic spasms syndrome and autism spectrum disorder with an RFX3 mutation.

Torio, Michiko; Maeda, Kenichi; Akamine, Satoshi; Kawakami, Saori; Matsubara, Yoshie; Miya, Fuyuki; Kato, Mitsuhiro; Kira, Ryutaro.

Afiliação

Torio M; Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan; Department of General Pediatrics and Interdisciplinary Medicine, Fukuoka Children's Hospital, Fukuoka, Japan. Electronic address: toriomichiko@gmail.com.
Maeda K; Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan.
Akamine S; Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan.
Kawakami S; Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan.
Matsubara Y; Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan.
Miya F; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Kato M; Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan.
Kira R; Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan.

Seizure ; 112: 11-14, 2023 11.

Article em En | MEDLINE | ID: mdl-37717291