Developmental Foix‐Chavany‐Marie syndrome in identical twins

Neill R. Graff‐Radford, E. Peter Bosch, John C. Stears, Daniel Tranel

Research output: Contribution to journalArticlepeer-review

80 Scopus citations


Foix, Chavany, and Marie described a syndrome of faciopharyngoglossomasticatory diplegia resulting from bilateral anterior opercular infarction. We describe identical twins who have a developmental form of the syndrome. The twins, aged 41 years, were the product of a normal pregnancy and birth, but had subsequent delayed motor milestones, seizures, poor language development, mild mental retardation, drooling, absent gag reflexes, inability to protrude the tongue, briskk jaw jerks, impaired fine finger movements, symmetrical brisk reflexes, flexor plantar responses, and mildly spastic gait. Magnetic resonance imaging showed bilateral perisylvian cortical dysplasia compatible with polymicrogyria and incomplete opercula formation.

Original languageEnglish (US)
Pages (from-to)632-635
Number of pages4
JournalAnnals of neurology
Issue number5
StatePublished - Nov 1986

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology


Dive into the research topics of 'Developmental Foix‐Chavany‐Marie syndrome in identical twins'. Together they form a unique fingerprint.

Cite this