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PMID: 29080631 Published · ppublish English Journal Article Review

Ophthalmic manifestations in neurofibromatosis type 1.

Survey of ophthalmology ·Vol. 63 ·No. 4 ·2018-00-00 ·页码 518-533

Kinori M, Hodgson N, Zeid JL

Abstract

Neurofibromatosis type 1 (NF1) is a relatively common multisystemic inherited disease and has been extensively studied by multiple disciplines. Although genetic testing and confirmation are available, NF1 remains a clinical diagnosis. Many manifestations of NF1 involve the eye and orbit, and the ophthalmologist, therefore, plays a significant role in the diagnosis and treatment of NF1 patients. Improvements in diagnostic and imaging instruments have provided new insight to study the ophthalmic manifestations of the disease. We provide a comprehensive and up-to-date overview of the ocular and orbital manifestations of NF1.

Keywords
Lisch nodules neurofibromatosis type 1 optic pathway gliomas plexiform neurofibromas von Recklinghausen's disease
MeSH 主题词
Anterior Eye Segment/pathology Antineoplastic Agents/therapeutic use Eye Diseases/diagnosis,etiology,pathology Humans Neurofibromatosis 1/complications,diagnosis,therapy Ophthalmologic Surgical Procedures/methods Orbital Diseases/etiology,pathology,therapy Radiotherapy/methods
化学物质
Antineoplastic Agents
作者与单位
共 3 位作者,点击展开单位 / ORCID
Kinori Michael
Department of Ophthalmology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Hodgson Nickisa
Department of Ophthalmology, Shiley Eye Institute, University of California, San Diego, California, USA.
Zeid Janice Lasky
Department of Ophthalmology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA. Electronic address: jlaskyzeid@luriechildrens.org.
Article Info
Journal
Survey of ophthalmology
Abbr.
Surv Ophthalmol
ISSN
1879-3304
Published
2018-00-00
电子出版
2017-00-16
页码
518-533
Language
English
Country/Region
United States
NLM ID
0404551
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