Ophthalmic manifestations in neurofibromatosis type 1.
Surv Ophthalmol
; 63(4): 518-533, 2018.
Article
in En
| MEDLINE
| ID: mdl-29080631
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.
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Orbital Diseases
/
Neurofibromatosis 1
/
Eye Diseases
Type of study:
Diagnostic_studies
/
Etiology_studies
Limits:
Humans
Language:
En
Journal:
Surv Ophthalmol
Year:
2018
Document type:
Article
Affiliation country:
United States
Country of publication:
United States