Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10215382 | European Journal of Paediatric Neurology | 2018 | 4 Pages |
Abstract
Patients with early-onset FSHD generally had a severe phenotype compared to classical onset FSHD. However, after 22 years of follow up they showed a wide variation in severity and, despite these physical limitations, participated socially and economically. These observations are important for patient management and should be taken into account in clinical trials.
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Authors
Rianne J.M. Goselink, Caroline R. van Kernebeek, Karlien Mul, Richard J.L.F. Lemmers, Silvère M. van der Maarel, Oebele F. Brouwer, Nicol Voermans, George W. Padberg, Corrie E. Erasmus, Baziel G.M. van Engelen,