Familial cases with MECP2 microdeletion and gastroesophageal reflux, apnea and sick sinus syndrome

Takehiko Inui

Presentation information

Oral Presentation

Hereditary disorder/Chromosomal aberration

[O19] Hereditary disorder/Chromosomal aberration

Fri. Jun 1, 2018 11:00 AM - 11:50 AM Room 7 (3F 304)

Chair:Takahito WADA(Kyoto University Graduate School of Medicine, Department of Medical Ethics and Medical Genetics), Nobuyuki Murakami(Dokkyo Medical University, Saitama Medical Center, Department of Pediatrics)

[O-103] Familial cases with MECP2 microdeletion and gastroesophageal reflux, apnea and sick sinus syndrome

Takehiko Inui¹, TAKUYA MIYABAYASHI¹, RYO SATO¹, YUKIMUNE OHKUBO¹, NORIKO TOGASHI¹, KAZUHIRO IWAMA², TSUYOSHI MIZUGUCHI², NAOMICHI MATSUMOTO², KAZUHIRO HAGINOYA¹ (1.Department of Pediatric Neurology, Miyagi Children's Hospital, Miyagi, Japan, 2.Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan)

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