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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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| Publicado en: | Indian J Ophthalmol |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5621276/ https://ncbi.nlm.nih.gov/pubmed/28905837 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijo.IJO_303_17 |
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