Case Reports
doi: 10.1212/wnl.51.5.1500.
Polymicrogyria in chromosome 22 delection syndrome
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- PMID: 9818897
- DOI: 10.1212/wnl.51.5.1500
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Case Reports
Polymicrogyria in chromosome 22 delection syndrome
Neurology.
1998 Nov.
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.
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