Epilepsy and migraine in a patient with Urbach-Wiethe disease

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

doi:10.1016/j.seizure.2007.02.014

Epilepsy and migraine in a patient with Urbach-Wiethe disease

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

Research output: Contribution to journal › Article › peer-review

19 Citations (Scopus)

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.

Original language	English
Pages (from-to)	465-468
Number of pages	4
Journal	Seizure
Volume	16
Issue number	5
DOIs	https://doi.org/10.1016/j.seizure.2007.02.014
Publication status	Published - 1 Jul 2007
Externally published	Yes

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10.1016/j.seizure.2007.02.014

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title = "Epilepsy and migraine in a patient with Urbach-Wiethe disease",

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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AU - Claeys, Kristl G.

AU - Claes, Lieve R.F.

AU - Van Goethem, Johan W.M.

AU - Sercu, Sandy

AU - Merregaert, Joseph

AU - Lambert, Julien

AU - Van Marck, Eric A.

AU - Parizel, Paul M.

AU - De Jonghe, Peter

PY - 2007/7/1

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N2 - 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.

AB - 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.

KW - Cerebral calcifications

KW - Epilepsy

KW - Migraine

KW - Partial seizures

KW - Topiramate

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ER -

Epilepsy and migraine in a patient with Urbach-Wiethe disease

Abstract

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