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Updated: Jul 27, 2026

Spectral Karyotyping to Study Chromosome Abnormalities in Humans and Mice with Polycystic Kidney Disease
Published on: February 3, 2012
Polymicrogyria in chromosome 22 delection syndrome
P M Bingham1, D Lynch, D McDonald-McGinn
1Division of Neurology, Children's Hospital of Philadelphia, PA 19104, USA.
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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