"Corneal Opacity" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque.
| Descriptor ID |
D003318
|
| MeSH Number(s) |
C11.204.299
|
| Concept/Terms |
Corneal Opacity- Corneal Opacity
- Corneal Opacities
- Opacities, Corneal
- Opacity, Corneal
- Leukoma
- Leukomas
|
Below are MeSH descriptors whose meaning is more general than "Corneal Opacity".
Below are MeSH descriptors whose meaning is more specific than "Corneal Opacity".
This graph shows the total number of publications written about "Corneal Opacity" by people in this website by year, and whether "Corneal Opacity" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 1 | 2 |
| 2001 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2014 | 0 | 1 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
| 2024 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Corneal Opacity" by people in Profiles.
-
Addressing corneal opacity after herpes zoster infection. J Cataract Refract Surg. 2024 Jun 01; 50(6):655-659.
-
Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism. Am J Hum Genet. 2020 02 06; 106(2):272-279.
-
Desmin deficiency is not sufficient to prevent corneal fibrosis. Exp Eye Res. 2019 03; 180:155-163.
-
Correlation Between Clinical Examination and Diagnostic Imaging in Type II Peters Anomaly. J Pediatr Ophthalmol Strabismus. 2017 Nov 01; 54(6):395.
-
Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes. Am J Med Genet A. 2016 10; 170(10):2711-8.
-
April consultation #4. J Cataract Refract Surg. 2015 Apr; 41(4):897; discussion 899.
-
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations. Am J Hum Genet. 2014 Jun 05; 94(6):915-23.
-
Atypical corneal immunoglobulin deposition in a patient with dysproteinemia. Cornea. 2010 Jan; 29(1):105-7.
-
Corneal epithelial opacity in dysfunctional tear syndrome. Am J Ophthalmol. 2009 Sep; 148(3):376-82.
-
Corneal wound healing after laser in situ keratomileusis flap lift and epithelial abrasion. J Cataract Refract Surg. 2003 Oct; 29(10):2007-12.