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Start free with EleplanPolymicrogyria
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
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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