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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Main Authors: Ammar M. Al Mahmood, Hind M. Al Katan, Ghada Y. Al Bin Ali, Samar A. Al-Swailem
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Case Reports in Ophthalmological Medicine
Online Access:http://dx.doi.org/10.1155/2012/573045
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spelling 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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