[P21] Metabolic diseaseLysosomal storage disease

[P-117] Urinary mulberry cells observed in one Fabry disease boy with normal kidney function

Pin Fee Chong^1,2, Fumiya Yamashita¹, Kenichi Maeda¹, Ryoko Nakamura¹, Kimitoshi Nakamura³, Ryutaro Kira¹ (1.Department of Pediatric Neurology, Fukuoka Children's Hospital, Fukuoka, Japan, 2.Department of General Pediatrics and Interdiscplinary Medicine, 3.Department of Pediatrics, Kumamoto University, Kumamoto, Japan)