Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome

Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant condition characterized by the dysgenesis of the anterior segment along with some systemic abnormalities such as dental and facial bone defects. Its incidence is thought to be 1 in 200,000. Treatment is predominantly the management of glauc...

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Detalles Bibliográficos
Autores principales: Khan, Taimoor A, Zahid, Muhammad A, Akram, Amjad, Rauf, Abdul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Ophthalmology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206113/
https://www.ncbi.nlm.nih.gov/pubmed/35733478
http://dx.doi.org/10.7759/cureus.25128

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206113/
https://www.ncbi.nlm.nih.gov/pubmed/35733478
http://dx.doi.org/10.7759/cureus.25128

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