Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics
Marcy C Speer1, David S Enterline, Lorraine Mehltretter
1Duke University Medical Center, Durham, North Carolina, marcy@chg.duhs.duke.edu.
Journal of Genetic Counseling
|July 5, 2015
Abstract:
Chiari type I malformation has traditionally been defined as a downward herniation of the cerebellar tonsils of ≥5 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.


