Epilepsy in individuals with neurofibromatosis type 1.
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| Title: | Epilepsy in individuals with neurofibromatosis type 1. |
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| Authors: | Ostendorf, Adam P., Gutmann, David H., Weisenberg, Judith L. Z. |
| Source: | Epilepsia (Series 4). Oct2013, Vol. 54 Issue 10, p1810-1814. 5p. |
| Subjects: | Epilepsy, Neurofibromatosis, Spasms, Medical records, Magnetic resonance imaging, Gliomas, Surgery |
| Abstract: | Purpose To describe the clinical characteristics and outcomes of individuals with neurofibromatosis type 1 ( NF1) and seizures in the largest cohort reported to date. Methods A retrospective cross-sectional review of 536 individuals with NF1 was performed, and clinical data from 51 individuals with a history of at least one seizure were analyzed. Key Findings In individuals with NF1, 9.5% had a history of at least one unprovoked seizure, and 6.5% had documented epilepsy. Individuals with seizures were more likely to have inherited NF1 from their mother (p = 0.001). Focal seizures were the most common type, occurring in 57% of individuals, although generalized seizures, specific electroclinical syndromes, and the presence of multiple seizure types were also noted. Moreover, in 21% of individuals with a previously unremarkable magnetic resonance imaging ( MRI) study, neuroimaging at seizure onset revealed a new structural abnormality. In this population, 77% of individuals required multiple antiepileptic drugs ( AEDs), and some required epilepsy surgery, with the best results following temporal lobe glioma resection. Significance Compared to the general population, seizures are more common in individuals with NF1, where they are often focal and related to an intracranial neoplasm. These observations suggest that all individuals with NF1 and a new seizure should undergo MRI despite previous normal neuroimaging. Individuals with seizures and NF1 typically require more aggressive therapy than those without NF1 and should be considered for epilepsy surgery when appropriate. [ABSTRACT FROM AUTHOR] |
| Copyright of Epilepsia (Series 4) is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 90525969 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Epilepsy in individuals with neurofibromatosis type 1. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ostendorf%2C+Adam+P%2E%22">Ostendorf, Adam P.</searchLink><br /><searchLink fieldCode="AR" term="%22Gutmann%2C+David+H%2E%22">Gutmann, David H.</searchLink><br /><searchLink fieldCode="AR" term="%22Weisenberg%2C+Judith+L%2E+Z%2E%22">Weisenberg, Judith L. Z.</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Epilepsia+%28Series+4%29%22">Epilepsia (Series 4)</searchLink>. Oct2013, Vol. 54 Issue 10, p1810-1814. 5p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Epilepsy%22">Epilepsy</searchLink><br /><searchLink fieldCode="DE" term="%22Neurofibromatosis%22">Neurofibromatosis</searchLink><br /><searchLink fieldCode="DE" term="%22Spasms%22">Spasms</searchLink><br /><searchLink fieldCode="DE" term="%22Medical+records%22">Medical records</searchLink><br /><searchLink fieldCode="DE" term="%22Magnetic+resonance+imaging%22">Magnetic resonance imaging</searchLink><br /><searchLink fieldCode="DE" term="%22Gliomas%22">Gliomas</searchLink><br /><searchLink fieldCode="DE" term="%22Surgery%22">Surgery</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Purpose To describe the clinical characteristics and outcomes of individuals with neurofibromatosis type 1 ( NF1) and seizures in the largest cohort reported to date. Methods A retrospective cross-sectional review of 536 individuals with NF1 was performed, and clinical data from 51 individuals with a history of at least one seizure were analyzed. Key Findings In individuals with NF1, 9.5% had a history of at least one unprovoked seizure, and 6.5% had documented epilepsy. Individuals with seizures were more likely to have inherited NF1 from their mother (p = 0.001). Focal seizures were the most common type, occurring in 57% of individuals, although generalized seizures, specific electroclinical syndromes, and the presence of multiple seizure types were also noted. Moreover, in 21% of individuals with a previously unremarkable magnetic resonance imaging ( MRI) study, neuroimaging at seizure onset revealed a new structural abnormality. In this population, 77% of individuals required multiple antiepileptic drugs ( AEDs), and some required epilepsy surgery, with the best results following temporal lobe glioma resection. Significance Compared to the general population, seizures are more common in individuals with NF1, where they are often focal and related to an intracranial neoplasm. These observations suggest that all individuals with NF1 and a new seizure should undergo MRI despite previous normal neuroimaging. Individuals with seizures and NF1 typically require more aggressive therapy than those without NF1 and should be considered for epilepsy surgery when appropriate. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Epilepsia (Series 4) is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/epi.12348 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1810 Subjects: – SubjectFull: Epilepsy Type: general – SubjectFull: Neurofibromatosis Type: general – SubjectFull: Spasms Type: general – SubjectFull: Medical records Type: general – SubjectFull: Magnetic resonance imaging Type: general – SubjectFull: Gliomas Type: general – SubjectFull: Surgery Type: general Titles: – TitleFull: Epilepsy in individuals with neurofibromatosis type 1. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ostendorf, Adam P. – PersonEntity: Name: NameFull: Gutmann, David H. – PersonEntity: Name: NameFull: Weisenberg, Judith L. Z. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: Oct2013 Type: published Y: 2013 Identifiers: – Type: issn-print Value: 00139580 Numbering: – Type: volume Value: 54 – Type: issue Value: 10 Titles: – TitleFull: Epilepsia (Series 4) Type: main |
| ResultId | 1 |