Literature DB >> 7567251

MRI of congenital Foix-Chavany-Marie syndrome.

M Cellerini1, M Mascalchi, F Salvi, G C Muscas, G Dal Pozzo.   

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.

Entities:  

Mesh：

Year:  1995        PMID： 7567251     DOI： 10.1007/BF02011116

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


  4 in total

Review 1.  Formation, maturation, and disorders of brain neocortex.

Authors:  A J Barkovich; P Gressens; P Evrard
Journal:  AJNR Am J Neuroradiol       Date:  1992 Mar-Apr       Impact factor: 3.825

2.  Bilateral opercular polymicrogyria.

Authors:  P S Becker; A M Dixon; J C Troncoso
Journal:  Ann Neurol       Date:  1989-01       Impact factor: 10.422

3.  Bilateral central macrogyria: epilepsy, pseudobulbar palsy, and mental retardation--a recognizable neuronal migration disorder.

Authors:  R Kuzniecky; F Andermann; D Tampieri; D Melanson; A Olivier; I Leppik
Journal:  Ann Neurol       Date:  1989-06       Impact factor: 10.422

4.  Developmental Foix-Chavany-Marie syndrome in identical twins.

Authors:  N R Graff-Radford; E P Bosch; J C Stears; D Tranel
Journal:  Ann Neurol       Date:  1986-11       Impact factor: 10.422
  4 in total

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