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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Detalles Bibliográficos
Autores principales: Asano, Mamika, Tsukamoto, Shoko, Sonoda, Koh-Hei, Kondo, Hiroyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220311/
https://www.ncbi.nlm.nih.gov/pubmed/34189343
http://dx.doi.org/10.1016/j.ajoc.2021.101137

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220311/
https://www.ncbi.nlm.nih.gov/pubmed/34189343
http://dx.doi.org/10.1016/j.ajoc.2021.101137

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