| Literature DB >> 29080631 |
Michael Kinori1, Nickisa Hodgson2, Janice Lasky Zeid3.
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.Entities:
Keywords: Lisch nodules; neurofibromatosis type 1; optic pathway gliomas; plexiform neurofibromas; von Recklinghausen's disease
Mesh:
Substances:
Year: 2017 PMID: 29080631 DOI: 10.1016/j.survophthal.2017.10.007
Source DB: PubMed Journal: Surv Ophthalmol ISSN: 0039-6257 Impact factor: 6.048