What causes MPS VI ............................................................ Are there different forms of MPS VI? .................................... How common is MPS

Case Report Fundoscopic Changes in Maroteaux-Lamy Syndrome Augusto Magalhães,1 Jorge Meira ,1 Ana Maria Cunha,1 Raul Jorge Moreira,1 Elisa Leão-Teles,2 Manuel

Expert and patient meeting on Maroteaux Lamy disease (MPS VI) 15–16 October 2016 Hilton, Northampton Programme and booking form The MPS Society is holding an expert

J. Int Oral Health 2010 Case Report All right reserved JIOH, August 2010, Volume 2 (Issue 2) Page 1 Maroteaux-Lamy Mucopolysaccharidosis *Associate Professor, **Lecturer,

EU_Ophthalmic_cover.qxpLysosomal storage disorders (LSDs) are a group of more than 50 inheritable disorders.1,2 Although individually rare, they collectively affect approximately

Slide 1Lessons Learned from MEPSEVII: Enzyme Replacement Therapy for MPS VII Dina J. Zand, MD Division of Gastroenterology and Inborn Errors Products (DGIEP) U.S. Food and

10545_2015_9895_Article 285..292Long-term cognitive follow-up in children treated for Maroteaux-Lamy syndrome Berendine J. Ebbink1 & Marion M. G. Brands1 & Johanna

University Of MinnesotaMT2014-08R Co-Investigators: Paul Orchard, MD *Co-I’s who will not consent subjects Biostatistician: Qing Cao, MS Confidential December 4, 2015

Bone marrow transplantation for Maroteaux–Lamy syndrome (MPS VI): Long-term follow-upJ. Inher. Metab. Dis. 22 50È62(1999) SSIEM and Kluwer Academic Publishers.

Mucopolysaccharidosis type VIMucopolysaccharidosis type VI Description Mucopolysaccharidosis type VI (MPS VI), also known as Maroteaux-Lamy syndrome, is a progressive condition