En face optical coherence tomography findings in a case of Alport syndrome

Alport syndrome is a rare hereditary disease that is associated with retinal abnormalities such as dot-and-fleck retinopathy and temporal macular thinning. The main pathophysiological process of Alport syndrome is loss of the collagen network in the basement membrane. However, the alterations in eac...

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Detalles Bibliográficos
Autores principales: Cho, In Hwan, Kim, Hoon Dong, Jung, Sang Joon, Park, Tae Kwann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Brief Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621276/
https://www.ncbi.nlm.nih.gov/pubmed/28905837
http://dx.doi.org/10.4103/ijo.IJO_303_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621276/
https://www.ncbi.nlm.nih.gov/pubmed/28905837
http://dx.doi.org/10.4103/ijo.IJO_303_17

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