| Literature DB >> 17403608 |
Kristl G Claeys1, 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.
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.Entities:
Mesh：
Year: 2007 PMID： 17403608 DOI： 10.1016/j.seizure.2007.02.014
Source DB: PubMed Journal: Seizure ISSN： 1059-1311 Impact factor: 3.184