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Society for Pediatric Radiology – Poster Archive


Mucopolysaccharidoses
Showing 1 Abstract.

Matsubara Yoshiko,  Miyazaki Osamu,  Nosaka Shunsuke,  Kosuga Motomichi,  Okuyama Torayuki,  Awai Kazuo

Final Pr. ID: Poster #: SCI-002

Enzyme replacement therapy (ERT) is approved for the treatment of mucopolysaccharidoses (MPS) I: Hurler syndrome (IH), Hurler-Scheie syndrome (IHS) and Scheie syndrome (IS), II: Hunter syndrome, and VI: Maroteaux-Lamy syndrome. However, ERT is thought to have no therapeutic effect on the central nervous system (CNS) because the enzyme could not permeate through the blood-brain barrier (BBB). We aimed to assess CNS involvement in MPS at the start of ERT and to evaluate the interval changes demonstrated on magnetic resonance imaging (MRI) over a long-term follow up. Read More

Authors:  Matsubara Yoshiko , Miyazaki Osamu , Nosaka Shunsuke , Kosuga Motomichi , Okuyama Torayuki , Awai Kazuo

Keywords:  mucopolysaccharidoses, enzymatic replacement therapy, magnetic resonance imaging