 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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 2 | 0 | 2 | | 2008 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2014 | 1 | 0 | 1 | | 2019 | 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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Farooq AV, Colby K. Contact Lenses in the Management of Corneal Dystrophies. Klin Monbl Augenheilkd. 2020 Feb; 237(2):175-179.
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Farooq AV, Tu EY, D'jalilian AR, Traish AS, Hou JH. Persistent staining of lattice lines after intraoperative trypan blue use in patients with lattice corneal dystrophy. Cornea. 2014 Nov; 33(11):1235-7.
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Nakamura H, Li FT, Foltermann MO, Macsai M, Ma X, Zhao XC, Flaherty K, Yee RW. Individual phenotypic variances in a family with Thiel-Behnke corneal dystrophy. Cornea. 2012 Nov; 31(11):1217-22.
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Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, Karkera J, Mahurkar S, Lisch W, Dupps WJ, White PS, Winters RS, Kim C, Rapuano CJ, Sutphin J, Reidy J, Hu FR, Lu DW, Ebenezer N, Nickerson ML. Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function. . 2008 Feb 01; 146A(3):271-83.
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Poulaki V, Colby K. Genetics of anterior and stromal corneal dystrophies. Semin Ophthalmol. 2008 Jan-Feb; 23(1):9-17.
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Chiu EK, Lin AY, Folberg R, Saidel M. Avellino dystrophy in a patient after laser-assisted in situ keratomileusis surgery manifesting as granular dystrophy. Arch Ophthalmol. 2007 May; 125(5):703-5.
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Ebenezer ND, Patel CB, Hariprasad SM, Chen LL, Patel RJ, Hardcastle AJ, Allen RC. Clinical and molecular characterization of a family with autosomal recessive cornea plana. Arch Ophthalmol. 2005 Sep; 123(9):1248-53.
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Sorour HM, Yee SB, Peterson NJ, Li FT, Macsai MS, Zhao XC, Yee RW. Recurrence of chromosome 10 Thiel-Behnke corneal dystrophy (CDB2) after excimer laser phototherapeutic keratectomy or penetrating keratoplasty. Cornea. 2005 Jan; 24(1):45-50.
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Liu NP, Baldwin J, Jonasson F, Dew-Knight S, Stajich JM, Lennon F, Pericak-Vance MA, Klintworth GK, Vance JM. Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I gene. Am J Hum Genet. 1998 Sep; 63(3):912-7.
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Liu NP, Baldwin J, Lennon F, Stajich JM, Thonar EJ, Pericak-Vance MA, Klintworth GK, Vance JM. Coexistence of macular corneal dystrophy types I and II in a single sibship. Br J Ophthalmol. 1998 Mar; 82(3):241-4.
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