Literature DB >> 8453842

The association of Chiari type I malformation and neurofibromatosis type 1.

J Dooley, D Vaughan, M Riding, P Camfield.   

Abstract

The association of neurofibromatosis type 1 (NF1) with Chiari malformations of the cerebellum and brain stem has been reported on only two previous occasions. The pathogenesis of both conditions has remained unclear, although the Chiari type I malformation is most likely due to hypoplasia of the posterior fossa with subsequent extension of the cerebellum through the foramen magnum. NF1 is also associated with a variety of cerebral dysplasias. We present a patient with both of these dysplastic lesions whose Chiari malformation was asymptomatic.

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Year:  1993        PMID: 8453842     DOI: 10.1177/000992289303200316

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN: 0009-9228            Impact factor:   1.168


  5 in total

1.  Pierre-Robin syndrome associated with Chiari I malformation.

Authors:  R Shane Tubbs; W Jerry Oakes
Journal:  Childs Nerv Syst       Date:  2003-12-05       Impact factor: 1.475

2.  Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics.

Authors:  Marcy C Speer; David S Enterline; Lorraine Mehltretter; Preston Hammock; Judith Joseph; Margaret Dickerson; Richard G Ellenbogen; Thomas H Milhorat; Michael A Hauser; Timothy M George
Journal:  J Genet Couns       Date:  2003-08       Impact factor: 2.537

3.  Neurofibromatosis type 1 and type I Chiari malformation: an unusual association.

Authors:  P A Battistella; G Perilongo; C Carollo
Journal:  Childs Nerv Syst       Date:  1996-06       Impact factor: 1.475

4.  Chiari malformation type I: what information from the genetics?

Authors:  Valeria Capra; Michele Iacomino; Andrea Accogli; Marco Pavanello; Federico Zara; Armando Cama; Patrizia De Marco
Journal:  Childs Nerv Syst       Date:  2019-08-05       Impact factor: 1.475

5.  Optic pathway glioma, scoliosis, Chiari type 1 malformation, and syringomyelia in a patient with neurofibromatosis type 1.

Authors:  Faruk Incecık; Herguner M Ozlem; Sakır Altunbasak
Journal:  J Neurosci Rural Pract       Date:  2013-08
  5 in total

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