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Revesz syndrome with bilateral retinal detachments successfully treated by pars plana vitrectomy
BACKGROUND: Revesz syndrome is a rare type of the dyskeratosis congenita spectrum disorder that is characterized by nail dystrophy, oral leukoplakia, and abnormal skin pigmentation. The retinal features are similar to those of exudative retinopathy with avascular areas of the peripheral retina. Ther...
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| Veröffentlicht in: | Am J Ophthalmol Case Rep |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Elsevier
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8220311/ https://ncbi.nlm.nih.gov/pubmed/34189343 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajoc.2021.101137 |
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