[P16] Epilepsy/Convulsion Diagnosis/Gene

[P-094] A patient with epileptic encephalopathy associated with highly abnormal EEG and a MED13L mutation

Tomoe Yanagishita^1,2, TAICHI IMAIZUMI^1,3, KEIKO YAMAMOTO-SHIMOJIMA¹, HIKARU KITAHARA⁴, KATSUMI IMAI⁴, TOSHIYUKI YAMAMOTO¹ (1.Institute of Medical Genetics, Tokyo Womens Medical University, Tokyo, Japan, 2.Department of Pediatrics, Tokyo Womens Medical University, Tokyo, Japan, 3.Department of Pediatrics, St. Marianna University School of Medicine, Kawasaki, Japan, 4.Department of Pediatrics, National Epilepsy Center Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan)