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Published on: June 2, 2014
Epilepsy and migraine in a patient with Urbach-Wiethe disease
Kristl G Claeys1, Lieve R F Claes, Johan W M Van Goethem
1Neurogenetics Group, Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology (VIB), University of Antwerp, Universiteitsplein 1, B-2610 Antwerpen, Belgium. kristl.claeys@ua.ac.be
Abstract:
We report the clinical, neuroradiological, and molecular genetic findings in a patient with lipoid proteinosis or Urbach-Wiethe disease. Interestingly, in this patient epilepsy and migraine were the symptoms leading to the diagnosis of the disease, contrary to most patients in whom skin abnormalities are the first recognized symptoms.
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