Sturge Weber Syndrome

Wednesday, April 20, 2016

In this podcast, Sloka Iyengar PhD, epilepsy.com basic science editor, discusses Sturge Weber Syndrome, also known as SWS and encephalotrigeminal angiomatosis. This rare condition is typically recognized at birth, has an estimated incidence of 1 in 50,000, and affects males and females equally. Learn more about Sturge Weber Syndrome.

Listen Here

 

About Dr. Iyengar

I am an epilepsy researcher and have been investigating mechanisms that cause neurons to generate and sustain spontaneous seizures. For my graduate work, I used electrophysiology to study epileptic circuits; as a postdoctoral fellow, I studied neurogenesis (the birth of new neurons in the adult brain) in the hippocampus. As a clinical researcher, I conducted clinical trials for people with epilepsy, and worked on projects related to brain tumor-related epilepsy and special issues in women with epilepsy. As the editor of the basic science section for epilepsy.com, I write and edit articles to make scientific discoveries about epilepsy more accessible to people with epilepsy and their caregivers. I also advocate for increased funding for neuroscience research on Capitol Hill. Visit me at www.slokaiyengar.com.

Authored by: Sloka Iyengar PhD | Basic Science Editor on 4/2016

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The mission of the Epilepsy Foundation is to lead the fight to overcome the challenges of living with epilepsy and to accelerate therapies to stop seizures, find cures, and save lives.

 
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