Corneal Dystrophies, Hereditary
"Corneal Dystrophies, Hereditary" 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.
Bilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect.
| Descriptor ID |
D003317
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| MeSH Number(s) |
C11.204.236 C11.270.162 C16.320.290.162
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| Concept/Terms |
Corneal Dystrophies, Hereditary- Corneal Dystrophies, Hereditary
- Corneal Dystrophy, Hereditary
- Dystrophies, Hereditary Corneal
- Dystrophy, Hereditary Corneal
- Hereditary Corneal Dystrophies
- Hereditary Corneal Dystrophy
Stromal Dystrophies, Corneal- Stromal Dystrophies, Corneal
- Corneal Stromal Dystrophies
- Corneal Stromal Dystrophy
- Dystrophies, Corneal Stromal
- Dystrophy, Corneal Stromal
- Stromal Dystrophy, Corneal
Granular Dystrophy, Corneal- Granular Dystrophy, Corneal
- Corneal Granular Dystrophies
- Corneal Granular Dystrophy
- Dystrophies, Corneal Granular
- Dystrophy, Corneal Granular
- Granular Dystrophies, Corneal
Macular Dystrophy, Corneal- Macular Dystrophy, Corneal
- Corneal Macular Dystrophies
- Corneal Macular Dystrophy
- Dystrophies, Corneal Macular
- Dystrophy, Corneal Macular
- Macular Dystrophies, Corneal
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Below are MeSH descriptors whose meaning is more general than "Corneal Dystrophies, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Corneal Dystrophies, Hereditary".
This graph shows the total number of publications written about "Corneal Dystrophies, Hereditary" by people in this website by year, and whether "Corneal Dystrophies, Hereditary" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Corneal Dystrophies, Hereditary" by people in Profiles.
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Lockhart CM, Smith TB, Yang P, Naidu M, Rettie AE, Nath A, Weleber R, Kelly EJ. Longitudinal characterisation of function and structure of Bietti crystalline dystrophy: report on a novel homozygous mutation in CYP4V2. Br J Ophthalmol. 2018 02; 102(2):187-194.
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Lockhart CM, Nakano M, Rettie AE, Kelly EJ. Generation and characterization of a murine model of Bietti crystalline dystrophy. Invest Ophthalmol Vis Sci. 2014 Aug 12; 55(9):5572-81.
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Kelly EJ, Nakano M, Rohatgi P, Yarov-Yarovoy V, Rettie AE. Finding homes for orphan cytochrome P450s: CYP4V2 and CYP4F22 in disease states. Mol Interv. 2011 Apr; 11(2):124-32.
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Freedman J. Nama keratopathy. Br J Ophthalmol. 1973 Sep; 57(9):688-91.
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Freedman J. Survey of ocular disease among the Nama people of South West Africa. Br J Ophthalmol. 1973 Sep; 57(9):681-7.