Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/55556
Citations
Scopus Web of ScienceĀ® Altmetric
?
?
Type: Journal article
Title: Orbital plexiform neurofibroma and high axial myopia
Author: Chen, J.
Muecke, J.
Brown, S.
Citation: Ophthalmic Plastic and Reconstructive Surgery, 2008; 24(4):284-286
Publisher: Lippincott Williams & Wilkins
Issue Date: 2008
ISSN: 0740-9303
1537-2677
Statement of
Responsibility: 
Chen, JY; Muecke, JS and Brown, SD.
Abstract: PURPOSE: To report a group of children with neurofibromatosis type 1 and orbital plexiform neurofibroma who developed axial myopia in the associated eye. METHODS: The clinical records and imaging of 3 patients with neurofibromatosis type 1 and orbital plexiform neurofibromas were reviewed. RESULTS: Three patients were identified who were diagnosed with orbital plexiform neurofibromas at the ages of 10 months, 9 months, and 16 years old. In all cases the axial length of the eye associated with the neurofibroma increased with length compared with the unaffected eye over time. Accordingly, the affected eye became increasing myopic with age, while the unaffected eye remained emmetropic. CONCLUSIONS: Eyes affected with orbital plexiform neurofibroma, a hallmark of neurofibromatosis type 1, appear to be associated with increased axial length and myopia. This is of particular importance in children, to diagnose and treat unilateral high myopia early and prevent anisometropic amblyopia.
Keywords: Eye
Humans
Neurofibroma, Plexiform
Neurofibromatosis 1
Orbital Neoplasms
Myopia, Degenerative
Tomography, X-Ray Computed
Magnetic Resonance Imaging
Retinoscopy
Adolescent
Infant
Female
DOI: 10.1097/IOP.0b013e318177f116
Description (link): http://www.ncbi.nlm.nih.gov/pubmed/18645432
Published version: http://dx.doi.org/10.1097/iop.0b013e318177f116
Appears in Collections:Aurora harvest
Opthalmology & Visual Sciences publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.