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Concept information

Nervous System Diseases > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group III > Polymicrogyria
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Nervous System Malformations > Malformations of Cortical Development > Malformations of Cortical Development, Group III > Polymicrogyria

Terme préférentiel

Polymicrogyria  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Synonyme(s)

  • Cerebral Micropolygyria
  • Cerebral Polymicrogyria
  • Micropolygyria

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-FJGD8QK9-L

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RDF/XML TURTLE JSON-LD Date de création 26/06/2014, dernière modification le 01/07/2019