Neonatal status epilepticus controlled with levetiracetam at Sturge Weber syndrome.


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


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