Monitoring and Management of the Patient with Stargardt Disease

Stargardt disease (STGD1) represents one of the major common causes of inherited irreversible visual loss. Due to its high phenotypic and genotypic heterogeneity, STGD1 is a complex disease to understand. Non-invasive imaging, biochemical, and genetic advances have led to substantial improvements in...

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Detalles Bibliográficos
Autores principales: Cicinelli, Maria Vittoria, Battista, Marco, Starace, Vincenzo, Battaglia Parodi, Maurizio, Bandello, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886536/
https://www.ncbi.nlm.nih.gov/pubmed/31819694
http://dx.doi.org/10.2147/OPTO.S226595

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6886536/
https://www.ncbi.nlm.nih.gov/pubmed/31819694
http://dx.doi.org/10.2147/OPTO.S226595

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