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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

Término preferido

Polymicrogyria  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Etiquetas alternativas

  • Cerebral Micropolygyria
  • Cerebral Polymicrogyria
  • Micropolygyria

En otras lenguas

URI

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

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RDF/XML TURTLE JSON-LD Creado 26/6/14, última modificación 1/7/19