Document Detail


Comorbidity of epilepsy and headache in patients with Sturge-Weber syndrome.
MedLine Citation:
PMID:  16225815     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Sturge-Weber syndrome is associated with leptomeningeal angioma, trigeminal port-wine stain, epilepsy, and glaucoma. Clinically, many patients with Sturge-Weber syndrome are observed to have both seizures and headaches, but this has never been described in the literature. A questionnaire was mailed to 190 patients with reported comorbid epilepsy and headache as identified by the Sturge-Weber Foundation. Sixty-eight surveys were returned anonymously; 55 reported both seizures and headaches. The median age at headache onset was 8 years, with a median of three headaches per month. Fifty-eight percent felt that headaches were an equal or greater problem. Ibuprofen and acetaminophen were the most frequently tried abortive medications; 22% had tried sumatriptan. Only 22% reported a neurologist suggesting the use of an anticonvulsant as a preventive agent. Subjects with a family history of headaches had an earlier age at headache onset (7.5 vs 11 years; P = .02), and those with a family history of seizures were more likely to report behavior problems (69% vs 33%; P = .02). Subjects reporting learning problems or hemiparesis had an earlier age at seizure onset. Migraine-like headaches can be as significant a problem as epilepsy for patients with Sturge-Weber syndrome. Despite this, triptans and prophylactic medications (including anticonvulsants) were used in less than half of the patients. Correlations of family history with both age at symptom onset and behavior problems suggest that genetic substrate could be one factor determining the variable neurologic manifestations seen in Sturge-Weber syndrome.
Authors:
Eric H Kossoff; Laura A Hatfield; Karen L Ball; Anne M Comi
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Journal of child neurology     Volume:  20     ISSN:  0883-0738     ISO Abbreviation:  J. Child Neurol.     Publication Date:  2005 Aug 
Date Detail:
Created Date:  2005-10-17     Completed Date:  2006-02-24     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  8606714     Medline TA:  J Child Neurol     Country:  Canada    
Other Details:
Languages:  eng     Pagination:  678-82     Citation Subset:  IM    
Affiliation:
Department of Neurology, The Johns Hopkins Medical Institutions, Baltimore, MD, USA. ekossoff@jhmi.edu
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MeSH Terms
Descriptor/Qualifier:
Age of Onset
Anticonvulsants / therapeutic use
Child
Child Behavior Disorders / etiology
Child, Preschool
Comorbidity
Cross-Sectional Studies
Epilepsy / drug therapy,  etiology*,  genetics
Female
Genetic Predisposition to Disease
Headache / drug therapy,  etiology*
Humans
Male
Pedigree
Severity of Illness Index
Sturge-Weber Syndrome / complications*
Chemical
Reg. No./Substance:
0/Anticonvulsants

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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