Neonatal status epilepticus controlled with levetiracetam at Sturge Weber syndrome.

Abstract

Sturge-Weber syndrome is a rare, sporadic, congenital neurocutaneous syndrome characterized by facial cutaneous vascular malformation, leptomeningeal angioma and eye abnormalities. Seizures develop during the first year of life, may become refractory to multiple anticonvulsants and status epilepticus may develop. A rare subtype of Sturge-Weber syndrome with… (More)
DOI: 10.1016/j.braindev.2012.06.005

Topics

3 Figures and Tables

Slides referencing similar topics