| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 340840 | Seizure | 2007 | 4 Pages |
Abstract
SummaryWe 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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Authors
Kristl G. Claeys, Lieve R.F. Claes, Johan W.M. Van Goethem, Sandy Sercu, Joseph Merregaert, Julien Lambert, Eric A. Van Marck, Paul M. Parizel, Peter De Jonghe,