Walsh & Hoyt: STURGE-WEBER SYNDROME (ENCEPHALOTRIGEMINAL ANGIOMATOSIS)

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Identifier wh_ch38_1870-1878
Title Walsh & Hoyt: STURGE-WEBER SYNDROME (ENCEPHALOTRIGEMINAL ANGIOMATOSIS)
Creator John Kerrison, MD
Affiliation Retina Consultants of Charleston
Subject Sturge-Weber Syndrome; Encephalotrigeminal Angiomatosis
Description The two chief components of this syndrome are a cutaneous hemifacial angioma that usually stops at the midline and an ipsilateral angioma of the leptomeninges and brain. Other manifestations include partial seizures (83%), glaucoma (60%), and other neurologic deficits (65%) (611).
Date 2005
Language eng
Format application/pdf
Type Text
Source Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition
Relation is Part of Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology
Collection Neuro-Ophthalmology Virtual Education Library: Walsh and Hoyt Textbook Selections Collection: https://NOVEL.utah.edu
Publisher Wolters Kluwer Health, Philadelphia
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s61s0050
Setname ehsl_novel_whts
ID 187423
Reference URL https://collections.lib.utah.edu/ark:/87278/s61s0050