De novo SCN1A mutations in migrating partial seizures of infancy

D. Carranza Rojo, L. Hamiwka, J. M. McMahon, L. M. Dibbens, T. Arsov, A. Suls, T. Stödberg, K. Kelley, E. Wirrell, B. Appleton, M. MacKay, J. L. Freeman, S. C. Yendle, S. F. Berkovic, T. Bienvenu, P. De Jonghe, D. R. Thorburn, J. C. Mulley, H. C. Mefford, I. E. Scheffer

Research output: Contribution to journalArticlepeer-review

75 Scopus citations


Objective: To determine the genetic etiology of the severe early infantile onset syndrome of malignant migrating partial seizures of infancy (MPSI). Methods: Fifteen unrelated children with MPSI were screened for mutations in genes associated with infantile epileptic encephalopathies: SCN1A, CDKL5, STXBP1, PCDH19, and POLG. Microarray studies were performed to identify copy number variations. Results: One patient had a de novo SCN1A missense mutation p.R862G that affects the voltage sensor segment of SCN1A. A second patient had a de novo 11.06 Mb deletion of chromosome 2q24.2q31.1 encompassing more than 40 genes that included SCN1A. Screening of CDKL5 (13/15 patients), STXBP1 (13/15), PCDH19 (9/11 females), and the 3 common European mutations of POLG (11/15) was negative. Pathogenic copy number variations were not detected in 11/12 cases. Conclusion: Epilepsies associated with SCN1A mutations range in severity from febrile seizures to severe epileptic encephalopathies including Dravet syndrome and severe infantile multifocal epilepsy. MPSI is now the most severe SCN1A phenotype described to date. While not a common cause of MPSI, SCN1A screening should now be considered in patients with this devastating epileptic encephalopathy.

Original languageEnglish (US)
Pages (from-to)380-383
Number of pages4
Issue number4
StatePublished - Jul 26 2011

ASJC Scopus subject areas

  • Clinical Neurology


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