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 |