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Heterogeneous disorders of cortical malformation characterized by excessive and small fused gyri and shallow sulci of the CORTEX with abnormal cortical lamination. It is considered a malformation secondary to abnormal post-migrational development of the neurons during cerebral cortical development and is associated with EPILEPSY and learning difficulties.

Year introduced: 2015 (2008)

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Tree Number(s): C10.500.507.500.500, C16.131.666.507.500.500

MeSH Unique ID: D065706

Entry Terms:

  • Polymicrogyrias
  • Cerebral Polymicrogyria
  • Cerebral Polymicrogyrias
  • Polymicrogyria, Cerebral
  • Polymicrogyrias, Cerebral
  • Micropolygyria
  • Micropolygyrias
  • Cerebral Micropolygyria
  • Cerebral Micropolygyrias
  • Micropolygyria, Cerebral
  • Micropolygyrias, Cerebral

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