Search for a rare disease
Other search option(s)
Polymicrogyria
Disease definition
Polymicrogyria (PMG) 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
ORPHA:35981
Classification level: Group of disorders- Synonym(s): -
- Prevalence: Unknown
- Inheritance: Autosomal dominant or Autosomal recessive or X-linked dominant or Not applicable
- Age of onset: Childhood
- ICD-10: Q04.3
- OMIM: -
- UMLS: C0266464
- MeSH: -
- GARD: -
- MedDRA: -
Additional information
Further information on this disease
Health care resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.