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Epilepsy Gene Implicated in Severe Migraine Disorder

Northwestern Medicine scientists have discovered that mutations in the SCN2A gene, previously linked to epilepsy and autism, are also a hidden cause of a rare, severe form of migraine characterized by temporary one-sided paralysis. This finding reinforces the understanding of migraines as disorders of brain excitability and is expected to immediately improve genetic diagnosis and counseling for affected families.

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Personalized Brain Stimulation Offers New Hope for Drug-Resistant Epilepsy

A new study reveals that personalized deep brain stimulation shows significant promise for individuals with drug-resistant epilepsy, not only reducing seizures but also improving memory and sleep. By continuously monitoring brain activity with AI and adjusting stimulation in real-time, researchers at Mayo Clinic are paving the way for more effective and tailored treatments for this challenging condition.

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