Difference between revisions of "Fuchs dystrophy"
Jump to navigation
Jump to search
| (One intermediate revision by the same user not shown) | |||
| Line 1: | Line 1: | ||
'''Fuchs dystrophy''', also '''Fuchs endothelial dystrophy''', is a rare pathology of the [[eye]] that may be seen in ''Descemet's membrane'' specimens. | '''Fuchs dystrophy''', also '''Fuchs endothelial dystrophy''', is a rare pathology of the [[eye]] that may be seen in ''[[Descemet's membrane]]'' specimens. | ||
==General== | ==General== | ||
| Line 28: | Line 28: | ||
==See also== | ==See also== | ||
*[[Eye]]. | *[[Eye]]. | ||
*[[Pseudophakic bullous keratopathy]]. | |||
==References== | ==References== | ||
Latest revision as of 14:12, 13 October 2015
Fuchs dystrophy, also Fuchs endothelial dystrophy, is a rare pathology of the eye that may be seen in Descemet's membrane specimens.
General
- Uncommon.
Microscopic
Features:[1]
- Gutta.
- Accumulation of collagenous material from the basement membrane.
- Decreased endothelial density.[2]
- Thickening of Descemet's membrane.[3]
Images
Fuchs dystrophy. (WC)
www:
Sign out
Descemet’s Membrane, Right Eye, Excision: - Thickened Descemet’s membrane with marked decrease of endothelial cells and gutta consistent with Fuch's dystrophy.
See also
References
- ↑ McLaren, JW.; Bachman, LA.; Kane, KM.; Patel, SV. (Feb 2014). "Objective assessment of the corneal endothelium in Fuchs' endothelial dystrophy.". Invest Ophthalmol Vis Sci 55 (2): 1184-90. doi:10.1167/iovs.13-13041. PMID 24508788.
- ↑ 2.0 2.1 Klintworth, GK. (2009). "Corneal dystrophies.". Orphanet J Rare Dis 4: 7. doi:10.1186/1750-1172-4-7. PMID 19236704.
- ↑ URL: http://www.mrcophth.com/pathology/fuchendothelialdystrophy.html. Accessed on: 27 August 2015.
- ↑ 4.0 4.1 Shousha, MA.; Perez, VL.; Wang, J.; Ide, T.; Jiao, S.; Chen, Q.; Chang, V.; Buchser, N. et al. (Jun 2010). "Use of ultra-high-resolution optical coherence tomography to detect in vivo characteristics of Descemet's membrane in Fuchs' dystrophy.". Ophthalmology 117 (6): 1220-7. doi:10.1016/j.ophtha.2009.10.027. PMID 20163865.