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Retinoschisis associated with Kearns-Sayre syndrome

BACKGROUND: Kearns-Sayre Syndrome (KSS) is characterized by pigmentary retinopathy, external ophthalmoplegia and heart block. We report on a now 24-year-old male with clinical retinoschisis and molecularly confirmed KSS. MATERIALS AND METHODS: Physical and complete ophthalmic examination, molecular...

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Detalhes bibliográficos
Publicado no:Ophthalmic Genet
Main Authors: Chertkof, Julia, Hufnagel, Robert B., Blain, Delphine, Gropman, Andrea L., Brooks, Brian P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8127726/
https://ncbi.nlm.nih.gov/pubmed/32787478
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/13816810.2020.1799416
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