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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
Affiliation:(1) Duke University Medical Center, Durham, North Carolina;(2) Children's Hospital, Seattle, Washington;(3) The Chiari Institute, Manhasset, New York
Abstract:Chiari type I malformation has traditionally been defined as a downward herniation of the cerebellar tonsils of ge5 mm through the foramen magnum and it is likely associated with a volumetrically reduced posterior fossa. Syringomyelia is commonly associated with Chiari type I malformation. We estimate the prevalence of these two conditions and determine that they are more common than previously expected. We identify the genetic syndromes associated with some cases of Chiari type I malformation, and we provide evidence in favor of a genetic hypothesis for at least a subset of the nonsyndromic cases.
Keywords:Chiari type I malformation  syringomyelia  genetics  prevalence
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