[P21] Metabolic diseaseLysosomal storage disease

[P-121] A case of Congenital disorder of glycosylation typeII developed intracranial hemorrhage

Koji Tominaga^1,2, RYOKO HAYASHI¹, MIKA HIROTSUNE¹, JUNPEI TANIGAWA¹, YOSHIKO IWATANI^1,2, KURIKO SHIMONO^1,2, SHIN NABATAME¹, NAOKI KAGAWA³, KAZUHIKO BESSHO¹, TADASHI KANAME⁴, KEIICHI OZONO¹ (1.Department of Pediatrics, Graduate School of Medicine, Osaka University, Suita, Japan, 2.Division of Developmental Neuroscience, United Graduate School of Child Development, Osaka University, Suita, Japan, 3.Department of Neurosurgery, Graduate School of Medicine, Osaka University, Suita, Japan, 4.Department of Genome Medicine, National Center for Child Health and Development, Tokyo, Japan)