Polymicrogyria is an uncommon manifestation in 22q11.2 deletion syndrome

Am J Med Genet. 2000 Sep 4;94(1):77-8. doi: 10.1002/1096-8628(20000904)94:1<77::aid-ajmg16>3.0.co;2-v.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Brain / pathology
  • Chromosome Deletion*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 22*
  • Humans
  • Infant
  • Magnetic Resonance Imaging
  • Male
  • Syndrome