[Sturge-Weber syndrome in children. Clinical features, diagnosis and approaches to therapy on the example of three clinical cases].

Autor:	Shchederkina IO; Morozov Moscow children clinical hospital, Pediatric stroke center, Moscow, Russia., Livshtz MI; Morozov Moscow children clinical hospital, Pediatric stroke center, Moscow, Russia; Pirogov Russian National Research Medical University, Moscow, Russia., Kuzmina EV; Morozov Moscow children clinical hospital, Pediatric stroke center, Moscow, Russia., Seliverstova EV; Morozov Moscow children clinical hospital, Pediatric stroke center, Moscow, Russia., Kessel AE; Morozov Moscow children clinical hospital, Pediatric stroke center, Moscow, Russia., Petryaykina EE; Morozov Moscow children clinical hospital, Pediatric stroke center, Moscow, Russia; Russian University of Friendship, Moscow, Russia.
Jazyk:	ruština
Zdroj:	Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova [Zh Nevrol Psikhiatr Im S S Korsakova] 2019; Vol. 119 (11. Vyp. 2), pp. 55-64.
DOI:	10.17116/jnevro201911911255
Abstrakt:	Sturge-Weber syndrome belongs to the group of phacomotoses and is characterized by a combined lesion of the skin, eyes, nervous system and internal organs. The clinical course of Sturge-Weber syndrome is quite diverse. Of particular interest in the practice of pediatric neurology and neurosurgery is the fact that 72-90% of patients present with epilepsy. Of particular difficulty is the differential diagnosis of epileptic seizures and stroke-like episodes. The article presents clinical cases of patients with Sturge-Weber syndrome of various ages with epileptic seizures and transient ischemic attacks.
Databáze:	MEDLINE
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