Polymicrogyria in chromosome 22 delection syndrome.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 9818897.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
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.
Medical subject headings
- Brain
- Chromosome Deletion
- Chromosomes, Human, Pair 22
- Congenital Abnormalities