Polymicrogyria in chromosome 22 deletion syndrome
- 1 November 1998
- journal article
- Published by Wolters Kluwer Health in Neurology
- Vol. 51 (5) , 1500-1502
- https://doi.org/10.1212/wnl.51.5.1500
Abstract
We report two children with chromosome 22q11 deletion syndrome who had neuroradiologic evidence of polymicrogyria. The diagnosis of chromosome 22q11 deletion should be considered in individuals with polymicrogyria.Keywords
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