Ocular manifestations of Sturge–Weber syndrome: pathogenesis, diagnosis, and management
Open Access
- 1 May 2016
- journal article
- review article
- Published by Informa UK Limited in Clinical Ophthalmology
- Vol. ume 10, 871-878
- https://doi.org/10.2147/opth.s101963
Abstract
Ocular manifestations of SturgeâKeywords
This publication has 85 references indexed in Scilit:
- SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY EVIDENCE OF RETINAL NERVE FIBER LAYER AND GANGLION CELL LOSS IN ADULT PATIENTS WITH NEUROFIBROMATOSIS TYPE 1Retina, 2016
- Morphologic and vasculature features of the choroid and associated choroid–retinal thickness alterations in neurofibromatosis type 1British Journal of Ophthalmology, 2014
- 12-year retrospective study of Sturge-Weber syndrome and literature review.2014
- Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation inGNAQNew England Journal of Medicine, 2013
- Ruthenium-106 Plaque Therapy for Diffuse Choroidal Hemangioma in Sturge-Weber SyndromeCase Reports in Ophthalmological Medicine, 2011
- Sturge-Weber syndrome: A reviewPediatric Neurology, 2004
- Use of latanoprost in the treatment of glaucoma associated with Sturge-Weber syndromeAmerican Journal of Ophthalmology, 1998
- Low-dose external beam irradiation for bilateral diffuse choroidal hemangioma.1998
- Lethal genes surviving by mosaicism: A possible explanation for sporadic birth defects involving the skinJournal of the American Academy of Dermatology, 1987
- Combined trabeculotomy-trabeculectomy for the management of glaucoma associated wih Sturge-Weber syndrome.1981