bilateral polymicrogyria

Bilateral polymicrogyria is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

This condition is characterized by abnormal neuronal migration leading to a cerebral cortex with excessively small convolutions. Known symptoms include developmental delay, intellectual disability, and seizures. There are currently no orphan drug designations under investigation.

Patients and caregivers are encouraged to seek consultation with specialists experienced in neurological disorders. Genetic counseling may be beneficial, especially if there is a possibility of associated genetic syndromes. Connecting with rare disease registries and online patient communities can provide additional support and resources.