[P21] Metabolic diseaseLysosomal storage disease

[P-116] Long—term prognosis of enzyme replacement therapy in patients with infantile—onset Pompe disease

Hideaki Mashimo¹, Yohane Miyata¹, Ikuko Shirai¹, Satoko Kumada¹, Hiroya Nishida¹, Shumpei Uchino^1,2, Konomi Shimoda^1,2, Yasuo Hachiya^1,3, Eiji Kurihara¹ (1.The Department of Neurological pediatrics, Tokyo Metropolitan Neurology Hospital, Tokyo, Japan, 2.The department of Pediatrics, The university of Tokyo Hospital, Tokyo, Japan, 3.The department of Pediatrics, National Hospital organization Higashi-Nagano Hospital, Nagano, japan)