Neurotrophic keratitis in autoimmune polyglandular syndrome type 1: a case report

BACKGROUND: Autoimmune polyglandular syndrome type 1 (APS-1) is a rare autosomal recessive disease. In patients with APS-1, the most frequently reported ocular manifestations are keratoconjunctivitis with dry eye and retinal degeneration. However, to our knowledge, no research studies have reported...

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Detalles Bibliográficos
Autores principales: Wu, Po-Ying, Chang, Huai-Wen, Chen, Wei-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792334/
https://www.ncbi.nlm.nih.gov/pubmed/33413189
http://dx.doi.org/10.1186/s12886-020-01770-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7792334/
https://www.ncbi.nlm.nih.gov/pubmed/33413189
http://dx.doi.org/10.1186/s12886-020-01770-w

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