Polymicrogyria

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Polymicrogyria

ORPHA:35981Clinical group

What it is

A heterogenous group of cerebral cortical malformations characterized by excessive cortical folding and abnormal cortical layering that, depending on its topographic distribution, presents with variable combinations of neurological symptoms of varying severity such as epilepsy, developmental delay, intellectual disability, motor dysfunction (e.g. spasticity), and pseudobulbar palsy.

Key facts

Age of onset
Childhood
Inheritance
Autosomal dominant, Autosomal recessive, Not applicable, X-linked dominant
Classified as
Clinical group

Cross-references

MEDDRA 10073489MESH D065706MONDO 0000087MONDO 87UMLS C0266464

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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