A CASE OF STURGE-WEBER SYNDROME

A CASE OF STURGE-WEBER SYNDROME

Encephalo-trigeminal angiomatosis of Sturge-Weber-Krabbe-Dimitri is a rare hereditary sporadic facomatosis, characterized by the presence of angiomatosis of brain lining vessels, face and eye capillaries. We present the case of a 25-year old girl with a birth mark, an facial angioma localized in t...

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Bibliographic Details
Main Authors: Daniela Trasca, Vlad Claudiu Stefanescu, Inimioara Mihaela Cojocaru
Format: Article
Language:English
Published: Amaltea Medical Publishing House 2015-03-01
Series:Romanian Journal of Neurology
Subjects:
encephalo-trigeminal angiomatosis
sturge-weber syndrome
seizures
Online Access:https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2015-Nr.1/RJN_2015_1_Art-07.pdf

Internet

https://revistemedicale.amaltea.ro/Romanian_Journal_of_NEUROLOGY/Revista_Romana_de_NEUROLOGIE-2015-Nr.1/RJN_2015_1_Art-07.pdf

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