| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6016655 | European Journal of Paediatric Neurology | 2014 | 5 Pages |
Abstract
In conclusion, the presented case emphasizes that autoimmune disease is a recurrent feature of the Xp11.2 duplication syndrome, which should be considered in the follow-up of these patients. The exact mechanism underlying this autoimmune propensity remains to be elucidated.
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Authors
Sabine Verbeek, Olivier Vanakker, Rudy Mercelis, A.F. Lipka, Filomeen Haerynck, Melissa Dullaers, Patrick Verloo, Rudy Van Coster, Helene Verhelst,