MRI of congenital Foix-Chavany-Marie syndrome

M. Cellerini, M. Mascalchi, F. Salvi, G. C. Muscas, G. Dal Pozzo

Research output: Contribution to journalArticle

Abstract

MRI findings of bilateral central macrogyria allowed the diagnosis of a congenital variant of Foix-Chavany-Marie syndrome in four patients aged between 13 and 32 years, with facio-pharyngo-glosso-masticatory central diplegia, mental retardation and seizures.

Original languageEnglish
Pages (from-to)316-317
Number of pages2
JournalPediatric Radiology
Volume25
Issue number4
DOIs
Publication statusPublished - Jun 1995

ASJC Scopus subject areas

  • Radiological and Ultrasound Technology
  • Radiology Nuclear Medicine and imaging
  • Pediatrics, Perinatology, and Child Health

Fingerprint Dive into the research topics of 'MRI of congenital Foix-Chavany-Marie syndrome'. Together they form a unique fingerprint.

  • Cite this

    Cellerini, M., Mascalchi, M., Salvi, F., Muscas, G. C., & Dal Pozzo, G. (1995). MRI of congenital Foix-Chavany-Marie syndrome. Pediatric Radiology, 25(4), 316-317. https://doi.org/10.1007/BF02011116