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: NOVEL http://NOVEL.utah.edu
Publisher Wolters Kluwer Health, Philadelphia
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah, 10 N 1900 E SLC, UT 84112-5890
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
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