[P3] Congenital abnormality

[P-018] A case of Aicardi—Goutieres syndrome with persistent serum IFN—alpha elevation

Kazuo Kubota¹, HIDENORI OHNISHI¹, YOSHINORI TSURUSAKI², KENJI ORII³, TOSHIYUKI YAMAMOTO⁴, NAOMICHI MATSUMOTO², TOSHIYUKI FUKAO¹ (1.Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan, 2.Department of Human Genetics, Yokohama City University, Graduate School of Medicine, Yokohama, Japan, 3.Nagamori Pediatrics Clinic, 4.Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan, 5.Department of Developmental Disability Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan)