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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:
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
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author Khan, Taimoor A
Zahid, Muhammad A
Akram, Amjad
Rauf, Abdul
author_facet Khan, Taimoor A
Zahid, Muhammad A
Akram, Amjad
Rauf, Abdul
author_sort Khan, Taimoor A
collection PubMed
description 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 glaucoma and is mostly medical but can be surgical in refractory cases. Here, we describe the case of a 35-year-old female patient who presented with co-existing vernal keratoconjunctivitis and ARS. The treatment was more challenging as we had to manage two conditions simultaneously.
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spelling pubmed-92061132022-06-21 Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome Khan, Taimoor A Zahid, Muhammad A Akram, Amjad Rauf, Abdul Cureus Ophthalmology 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 glaucoma and is mostly medical but can be surgical in refractory cases. Here, we describe the case of a 35-year-old female patient who presented with co-existing vernal keratoconjunctivitis and ARS. The treatment was more challenging as we had to manage two conditions simultaneously. Cureus 2022-05-18 /pmc/articles/PMC9206113/ /pubmed/35733478 http://dx.doi.org/10.7759/cureus.25128 Text en Copyright © 2022, Khan et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Ophthalmology
Khan, Taimoor A
Zahid, Muhammad A
Akram, Amjad
Rauf, Abdul
Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome
title Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome
title_full Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome
title_fullStr Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome
title_full_unstemmed Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome
title_short Progressive Vision Loss in a Patient With Axenfeld-Rieger Syndrome
title_sort progressive vision loss in a patient with axenfeld-rieger syndrome
topic Ophthalmology
url 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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