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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Bibliographic Details
Published in:Am J Ophthalmol Case Rep
Main Authors: Asano, Mamika, Tsukamoto, Shoko, Sonoda, Koh-Hei, Kondo, Hiroyuki
Format: Artigo
Language:Inglês
Published: Elsevier 2021
Subjects:
Case Report
Online Access: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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