Neonatal status epilepticus controlled with levetiracetam at Sturge Weber syndrome
Makaleler > Tam Makale · 2013
Yazarlar: Sema TANRIVERDİ, Demet TEREK, Özge ALTUN, Mehmet YALAZ, Hasan TEKGÜL, NİLGÜN KÜLTÜRSAY
BRAIN & DEVELOPMENT, SCI Expanded İndekslerine Giren Dergi, Uluslararası, 2013, cilt 35, ss 367-371
DOI: 10.1016/j.braindev.2012.06.005
Özet
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 bilateral facial vascular malformation, unilateral cerebral involvement and neonatal status epilepticus is reported here. Neonatal status epilepticus was successfully controlled with intravenous levetiracetam infusion. (C) 2012 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.