NOVEL - Walsh and Hoyt Textbook
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Phacomatoses

Update Item Information
Title Walsh and Hoyt's Clinical Neuro-Ophthalmology
Subject Neurology; Ophthalmology; Eye Diseases
Description Walsh and Hoyt's Clinical Neuro-Ophthalmology
Date 2005
Language eng
Format application/pdf
Type Text
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Rights North American Neuro-Ophthalmology Association (NANOS), Copyright 2011. For further information regarding the rights to this collection, please visit http://library.med.utah.edu/NOVEL/about/copyright
ARK ark:/87278/s6rj4hsw
Setname ehsl_novel_wht
ID 190107
Reference URL https://collections.lib.utah.edu/ark:/87278/s6rj4hsw

Page Metadata

Identifier CH38_1823-1898
Title Phacomatoses
Alternative Title Section 8: Chapter 38
Creator John Kerrison, MD, Retina Consultants of Charleston
Affiliation Wilmer Eye Institute - Johns Hopkins Hospital
Subject Neurocutaneous Syndromes; Phacomatoses; Neurofibromatosis; Tuberous Sclerosis; Von Hippel-Lindau Disease; Sturge-Weber Syndrome; Ataxia; Wyburn-Mason Syndrome; Klippel-Trenaunay-Weber Syndrome
Description "Syndromes characterized by hamartomas of the skin, eye, central nervous system (CNS), and other viscera are collectivelycalled phacomatoses (1). These disorders produce significant visual and neurologic disturbances. Although most of these syndromes arise from mutations in single genes inherited in a Mendelian pattern, some have no apparent hereditarybasis. We discuss each of the syndromes considered in the categoryof neuro-ocular-cutaneous disorders."
Abstract "Syndromes characterized by hamartomas of the skin, eye, central nervous system (CNS), and other viscera are collectivelycalled phacomatoses (1). These disorders produce significant visual and neurologic disturbances. Although most of these syndromes arise from mutations in single genes inherited in a Mendelian pattern, some have no apparent hereditarybasis. We discuss each of the syndromes considered in the categoryof neuro-ocular-cutaneous disorders."
Language eng
Format application/pdf
Publication Type Book chapter
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Extent 4.5 MB
Setname ehsl_novel_wht
ID 190077
Reference URL https://collections.lib.utah.edu/ark:/87278/s6rj4hsw/190077