Walsh & Hoyt: Neurofibromatosis Type 1

Identifier wh_ch38_p1823_2
Title Walsh & Hoyt: Neurofibromatosis Type 1
Creator John Kerrison, MD
Affiliation Retina Consultants of Charleston
Subject Neurocutaneous Syndromes; Phacomatoses; Neurofibromatosis Type 1; Chiari Malformation
Description NF1 is one of the most common autosomal-dominant disorders. Artistic illustrations of the disease date back to the Middle Ages. Recognition as a distinct entity occurred with the report of von Recklinghausen in 1882. Since then, NF1 has been recognized to have protean manifestations that are characterized by cafe-au-lait spots, peripheral neurofibromas, and Lisch nodules
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/s6448vxm
Setname ehsl_novel_whts
ID 185766
Reference URL https://collections.lib.utah.edu/ark:/87278/s6448vxm
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