Achondroplasia Associated with Bilateral Keratoconus
We report a rare case of bilateral keratoconus in association with achondroplasia. A 26-year-old male, with a known case of achondroplasia, complained of bilateral gradual deterioration in vision for the past few years. Slit lamp biomicroscopy showed bilateral central corneal protrusion and stromal...
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2012-01-01
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Series: | Case Reports in Ophthalmological Medicine |
Online Access: | http://dx.doi.org/10.1155/2012/573045 |
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doaj-b3f33e4961744235ad62c5c3491286532020-11-24T22:53:43ZengHindawi LimitedCase Reports in Ophthalmological Medicine2090-67222090-67302012-01-01201210.1155/2012/573045573045Achondroplasia Associated with Bilateral KeratoconusAmmar M. Al Mahmood0Hind M. Al Katan1Ghada Y. Al Bin Ali2Samar A. Al-Swailem3Division of Anterior Segment, King Khaled Eye Specialist Hospital, Riyadh 11462, Saudi ArabiaDivision of Pathology, King Khaled Eye Specialist Hospital, Riyadh 11462, Saudi ArabiaDepartment of Ophthalmology, Bahrain Defence Force Hospital, West Riffa 28743, BahrainDivision of Anterior Segment, King Khaled Eye Specialist Hospital, Riyadh 11462, Saudi ArabiaWe report a rare case of bilateral keratoconus in association with achondroplasia. A 26-year-old male, with a known case of achondroplasia, complained of bilateral gradual deterioration in vision for the past few years. Slit lamp biomicroscopy showed bilateral central corneal protrusion and stromal thinning at the apex consistent with keratoconus. a trial of hard contact lens fitting failed to improve VA in the left eye (LE). Right eye (RE) improved to 20/25. The patient underwent penetrating keratoplasty (PKP) in his LE. Twenty-seven months postoperatively, uncorrected visual acuity (UCVA) was 20/30. Ophthalmologists should be aware that patients with achondroplasia who complain of poor vision should be suspected of having keratoconus once other more common conditions are ruled out.http://dx.doi.org/10.1155/2012/573045 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ammar M. Al Mahmood Hind M. Al Katan Ghada Y. Al Bin Ali Samar A. Al-Swailem |
spellingShingle |
Ammar M. Al Mahmood Hind M. Al Katan Ghada Y. Al Bin Ali Samar A. Al-Swailem Achondroplasia Associated with Bilateral Keratoconus Case Reports in Ophthalmological Medicine |
author_facet |
Ammar M. Al Mahmood Hind M. Al Katan Ghada Y. Al Bin Ali Samar A. Al-Swailem |
author_sort |
Ammar M. Al Mahmood |
title |
Achondroplasia Associated with Bilateral Keratoconus |
title_short |
Achondroplasia Associated with Bilateral Keratoconus |
title_full |
Achondroplasia Associated with Bilateral Keratoconus |
title_fullStr |
Achondroplasia Associated with Bilateral Keratoconus |
title_full_unstemmed |
Achondroplasia Associated with Bilateral Keratoconus |
title_sort |
achondroplasia associated with bilateral keratoconus |
publisher |
Hindawi Limited |
series |
Case Reports in Ophthalmological Medicine |
issn |
2090-6722 2090-6730 |
publishDate |
2012-01-01 |
description |
We report a rare case of bilateral keratoconus in association with achondroplasia. A 26-year-old male, with a known case of achondroplasia, complained of bilateral gradual deterioration in vision for the past few years. Slit lamp biomicroscopy showed bilateral central corneal protrusion and stromal thinning at the apex consistent with keratoconus. a trial of hard contact lens fitting failed to improve VA in the left eye (LE). Right eye (RE) improved to 20/25. The patient underwent penetrating keratoplasty (PKP) in his LE. Twenty-seven months postoperatively, uncorrected visual acuity (UCVA) was 20/30. Ophthalmologists should be aware that patients with achondroplasia who complain of poor vision should be suspected of having keratoconus once other more common conditions are ruled out. |
url |
http://dx.doi.org/10.1155/2012/573045 |
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