Ring chromosome 20 and epilepsy: a recognizable syndrome (two new cases)

Citation
A. Roubertie et al., Ring chromosome 20 and epilepsy: a recognizable syndrome (two new cases), REV NEUROL, 156(2), 2000, pp. 149-153
Citations number
29
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
REVUE NEUROLOGIQUE
ISSN journal
00353787 → ACNP
Volume
156
Issue
2
Year of publication
2000
Pages
149 - 153
Database
ISI
SICI code
0035-3787(200002)156:2<149:RC2AEA>2.0.ZU;2-T
Abstract
Ring chromosome 20 (RC20) is a rare chromosomopathy caracterized by slight mental deficiency, behavioral disorders and epilepsy. We report two cases o f ring chromosome 20, who exibited non convulsive: status epilepticus lasti ng minutes to hours, often triggered by emotional events, with associated t ypical electroencephalographic features. Our report-highlights the features of the electroclinical epilepsy syndrome associated with RC20, which repre sents a distinct and recognizable entity. The genetic basis of this disorde r is discussed.