Year: 2022
Type: article
Abstract: Sturge-weber syndrome (SWS), also known as encephalotrigeminal angiomatosis is a rare, congenital vascular disorder with as yet unknown causes, with no defined pattern of inheritance, characterized by a triad of flat facial angioma, leptomeningeal
Authors: Mario López-Monzón, Andrea Vivar, David Gallo, Alejandro Aguilar
Institution: Universidad de San Carlos de Guatemala
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: diamond
OpenAlex ID: W4295952094