Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures | Orphanet Journal of Rare Diseases | Full Text

Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures | Orphanet Journal of Rare Diseases | Full Text

Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures

Late-onset Pompe disease (LOPD) is a rare, hereditary, progressive disorder that is usually characterized by limb-girdle muscle weakness and/or respiratory insufficiency. LOPD is caused by mutations in the aci...

Authors:P. Vanherpe, S. Fieuws, A. D’Hondt, C. Bleyenheuft, P. Demaerel, J. De Bleecker, P. Van den Bergh, J. Baets, G. Remiche, K. Verhoeven, S. Delstanche, M. Toussaint, B. Buyse, P. Van Damme, C. E. Depuydt and K. G. Claeys

Citation:Orphanet Journal of Rare Diseases 2020 15:83

Content type:Research

Published on: 5 April 2020

• ViewFull Text
 
• ViewPDF