Fifty-two untreated patients with late-onset Pompe disease completed questionnaires about their clinical condition and level of handicap at baseline and at 1-year (n = 41) and 2-year follow-ups (n = 40). During this period, declines in functional activities, respiratory function, handicap, and survival were recorded on a group level. This study illustrates the progressiveness of late-onset Pompe disease and indicates the need for close clinical follow-up of both children and adults with this disorder. Copyright

doi.org/10.1212/01.wnl.0000198776.53007.2c, hdl.handle.net/1765/58121
Neurology
Department of Neurology

Hagemans, M., Hop, W., van Doom, P., Reuser, A., & van der Ploeg, A. (2006). Course of disability and respiratory function in untreated late-onset Pompe disease. Neurology, 66(4), 581–583. doi:10.1212/01.wnl.0000198776.53007.2c