Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1784729271549296640 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9206113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT khantaimoora progressivevisionlossinapatientwithaxenfeldriegersyndrome AT zahidmuhammada progressivevisionlossinapatientwithaxenfeldriegersyndrome AT akramamjad progressivevisionlossinapatientwithaxenfeldriegersyndrome AT raufabdul progressivevisionlossinapatientwithaxenfeldriegersyndrome |