Bilateral operculum syndrome

T. Lerman-Sagie*, E. Porat-Alkabetz, J. J. Meir, S. Harel

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

The bilateral operculum syndrome, is a unique developmental syndrome. It is characterized by spastic paralysis of the muscles of the face, pharynx, and of mastication, as well as by epilepsy and mental retardation. Imaging studies show bilateral, structural abnormalities in the frontal, perisylvian region consistent with polymicrogyria. These children are usually diagnosed as suffering from cerebral palsy, but in the bilateral operculum syndrome, intelligence is relatively preserved despite the severe motor involvement. Misdiagnosis may lead to improper estimation of rehabilitation potential preventing appropriate therapy, especially in the field of alternative communication. We present a 3-year-old boy, apparently the first case of this syndrome to be described in Israel.

Original languageEnglish
Pages (from-to)161-163, 215
JournalHarefuah
Volume131
Issue number5-6
StatePublished - 1996
Externally publishedYes

Fingerprint

Dive into the research topics of 'Bilateral operculum syndrome'. Together they form a unique fingerprint.

Cite this