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.
Publication types
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Case Reports
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Brain / abnormalities*
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Brain / pathology*
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Brain Stem / physiopathology
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Child, Preschool
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Chromosome Deletion*
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Chromosome Mapping
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Chromosomes, Human, Pair 22*
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Congenital Abnormalities / genetics*
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Congenital Abnormalities / pathology
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Congenital Abnormalities / physiopathology
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Electroencephalography
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Evoked Potentials, Auditory
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Humans
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Male
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Syndrome