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
|
| 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 |
|---|
| 1995 | 1 | 0 | 1 |
| 1997 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 2 | 0 | 2 |
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Below are the most recent publications written about "Corneal Dystrophies, Hereditary" by people in Profiles.
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Expert consensus on the identification, diagnosis, and treatment of neurotrophic keratopathy. BMC Ophthalmol. 2021 Sep 08; 21(1):327.
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Scleral Lens Use in Neurotrophic Keratopathy: A Review of Current Concepts and Practice. Eye Contact Lens. 2021 Mar 01; 47(3):144-148.
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Outcomes of corneal neurotisation using processed nerve allografts: a multicentre case series. Br J Ophthalmol. 2022 03; 106(3):326-330.
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Band keratopathy in children previously treated with diode laser for type 1 retinopathy of prematurity. J AAPOS. 2019 08; 23(4):232-234.
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April consultation #4. J Cataract Refract Surg. 2015 Apr; 41(4):897; discussion 899.
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Correlation between clinical in vivo confocal microscopic and ex vivo histopathologic findings of Salzmann nodular degeneration. Cornea. 2006 Jul; 25(6):734-8.
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[Schnyder corneal dystrophy and juvenile, systemic hypercholesteremia]. Klin Monbl Augenheilkd. 1997 Aug; 211(2):135-7.
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Impact of Salzmann's lesions on corneal curvature. J Cataract Refract Surg. 1995 Mar; 21(2):111-2.
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Unilateral lattice dystrophy of the cornea. Trans Am Acad Ophthalmol Otolaryngol. 1974 May-Jun; 78(3):OP440-4.
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Clinical observations on stimulus-deprivation amblyopia (amblyopia ex anopsia). Trans Am Ophthalmol Soc. 1967; 65:244-55.