LA05.50

ICD-11 MMS 2026-01

Polymicrogyria

Description

Polymicrogyria (PMG) is a cerebral cortical malformation characterised by excessive cortical folding and by shallow sulci. Microscopic examination reveals abnormal cortical layering. Topographic distribution of PMG is variable, but bilateral symmetrical perisylvian PMG (BPP) is the most frequent form. PMG is manifested by mild intellectual deficit, epilepsy, and pseudobulbar palsy, which causes difficulties with speech learning and feeding. The severity of PMG is highly dependent on the location and size of the affected area.

Index terms

  • Polymicrogyria
  • Bilateral polymicrogyria
  • Bilateral perisylvian polymicrogyria
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  • Bilateral frontoparietal polymicrogyria
  • Bilateral parasagittal parieto-occipital polymicrogyria
  • Bilateral frontal polymicrogyria
  • Bilateral generalised polymicrogyria
  • Unilateral polymicrogyria
  • Unilateral hemispheric polymicrogyria
  • Unilateral focal polymicrogyria

Exclusions from above levels

  • LD20.1 – Lissencephaly
  • LA01 – Encephalocele
  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

  • LA05.51 – Cortical dysplasia
  • LA05.5Y – Other specified abnormal neuronal migration
  • LA05.5Z – Abnormal neuronal migration, unspecified

Foundation entity

Polymicrogyria – http://id.who.int/icd/entity/2081858551

Part of: LA05.5: Abnormal neuronal migration › LA05: Cerebral structural developmental anomalies › 20: Developmental anomalies