Periventricular heterotopia associated with chromosome 5p anomalies

V. L. Sheen, J. W. Wheless, A. Bodell, E. Braverman, P. D. Cotter, Katherine A Rauen, O. Glenn, K. Weisiger, S. Packman, Christopher A. Walsh, E. H. Sherr

Research output: Contribution to journalArticle

85 Scopus citations

Abstract

Periventricular heterotopia (PH) is characterized by neuronal nodules along the lateral ventricles. Whereas mutations in X-linked FLNA cause such cortical malformations, the authors report two cases of PH localizing to chromosome 5p. Both subjects have complex partial seizures. MRI demonstrated bilateral nodular PH, with subcortical heterotopia or focal gliosis. FISH identified a duplication of 5p15.1 [46,XX,dup(5)(p15.1p15.1)] and a trisomy of 5p15.33 [46,XY,der(14)t(5; 14)(p15.33;p11.2) mat]. These findings suggest a new PH locus along the telomeric end of chromosome 5p.

Original languageEnglish (US)
Pages (from-to)1033-1036
Number of pages4
JournalNeurology
Volume60
Issue number6
StatePublished - Mar 25 2003
Externally publishedYes

ASJC Scopus subject areas

  • Clinical Neurology

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  • Cite this

    Sheen, V. L., Wheless, J. W., Bodell, A., Braverman, E., Cotter, P. D., Rauen, K. A., Glenn, O., Weisiger, K., Packman, S., Walsh, C. A., & Sherr, E. H. (2003). Periventricular heterotopia associated with chromosome 5p anomalies. Neurology, 60(6), 1033-1036.