Macular corneal dystrophy and associated corneal thinning
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25081284
PubMed Central
PMC4194335
DOI
10.1038/eye.2014.164
PII: eye2014164
Knihovny.cz E-resources
- MeSH
- Corneal Dystrophies, Hereditary genetics pathology MeSH
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Mutation * MeSH
- Corneal Pachymetry MeSH
- Cornea pathology MeSH
- Corneal Topography MeSH
- Carbohydrate Sulfotransferases MeSH
- Sulfotransferases genetics MeSH
- Organ Size MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Sulfotransferases MeSH
PURPOSE: To identify the molecular genetic cause of macular corneal dystrophy (MCD) in four probands, and characterize phenotypic similarities between MCD and keratoconus. METHODS: We performed ophthalmological examination, Scheimpflug imaging (Pentacam, Oculus Inc.), histopathological examination of excised corneal buttons, and direct sequencing of the CHST6 coding region. RESULTS: Pentacam measurements were taken in six eyes of three probands. All showed diffuse corneal thinning with paracentral steepening of the anterior corneal surface that was graded as keratoconus by the integrated software, but without associated ectasia of the posterior corneal surface or regional thinning. Homozygous or compound heterozygous CHST6 mutations were identified in all cases, including two novel mutations, c.13C>T; p.(Arg5Cys) and c.289C>T; p.(Arg97Cys). DISCUSSION: Localized elevation of the anterior corneal curvature can occur in MCD in the absence of other features of keratoconus. The identification of a further two Czech probands with the compound allele c.[484C>G; 599T>G] supports the enrichment of this allele in the study population.
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Klintworth GK. Corneal dystrophies. Orphanet J Rare Dis. 2009;4:7. PubMed PMC
Donnenfeld ED, Cohen EJ, Ingraham HJ, Poleski SA, Goldsmith E, Laibson PR. Corneal thinning in macular corneal dystrophy. Am J Ophthalmol. 1986;101:112–113. PubMed
Akama TO, Nishida K, Nakayama J, Watanabe H, Ozaki K, Nakamura T, et al. Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene. Nat Genet. 2000;26:237–241. PubMed
Ihalainen A. Clinical and epidemiological features of keratoconus genetic and external factors in the pathogenesis of the disease. Acta Ophthalmol Suppl. 1986;178:1–64. PubMed
Tuft SJ, Hassan H, George S, Frazer DG, Willoughby CE, Liskova P. Keratoconus in 18 pairs of twins. Acta Ophthalmol. 2012;90:e482–e486. PubMed
Cremona FA, Ghosheh FR, Rapuano CJ, Eagle RC, Jr, Hammersmith KM, Laibson PR, et al. Keratoconus associated with other corneal dystrophies. Cornea. 2009;28:127–135. PubMed
Lechner J, Dash DP, Muszynska D, Hosseini M, Segev F, George S, et al. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation. Invest Ophthalmol Vis Sci. 2013;54:3215–3223. PubMed
Liskova P, Veraitch B, Jirsova K, Filipec M, Neuwirth A, Ebenezer ND, et al. Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutation. Br J Ophthalmol. 2008;92:265–267. PubMed
Liskova P, Hysi PG, Williams D, Ainsworth JR, Shah S, de la Chapelle A, et al. Study of p.N247S KERA mutation in a British family with cornea plana. Mol Vis. 2007;13:1339–1347. PubMed
den Dunnen JT, Antonarakis SE. Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat. 2000;15:7–12. PubMed
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, et al. A method and server for predicting damaging missense mutations. Nat Methods. 2010;7:248–249. PubMed PMC
Li B, Krishnan VG, Mort ME, Xin F, Kamati KK, Cooper DN, et al. Automated inference of molecular mechanisms of disease from amino acid substitutions. Bioinformatics. 2009;25:2744–2750. PubMed PMC
Calabrese R, Capriotti E, Fariselli P, Martelli PL, Casadio R. Functional annotations improve the predictive score of human disease-related mutations in proteins. Hum Mutat. 2009;30:1237–1244. PubMed
Burdon KP, Vincent AL. Insights into keratoconus from a genetic perspective. Clin Exp Optom. 2013;96:146–154. PubMed
Javadi MA, Rafee'i AB, Kamalian N, Karimian F, Ja'farinasab MR, Yazdani S. Concomitant keratoconus and macular corneal dystrophy. Cornea. 2004;23:508–512. PubMed
Balestrazzi A, Martone G, Traversi C, Haka G, Toti P, Caporossi A. Keratoconus associated with corneal macular dystrophy: in vivo confocal microscopic evaluation. Eur J Ophthalmol. 2006;16:745–750. PubMed
Al-Hamdan G, Al-Mutairi S, Al-Adwani E, Al-Mujaini A. Bilateral coexistence of keratoconus and macular corneal dystrophy. Oman J Ophthalmol. 2009;2:79–81. PubMed PMC
Mohammad-Rabei H, Shojaei A, Aslani M. Concurrent macular corneal dystrophy and keratoconus. Middle East Afr J Ophthalmol. 2012;19:251–253. PubMed PMC
Tyynismaa H, Sistonen P, Tuupanen S, Tervo T, Dammert A, Latvala T, et al. A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families. Invest Ophthalmol Vis Sci. 2002;43:3160–3164. PubMed
Tomidokoro A, Oshika T, Amano S, Higaki S, Maeda N, Miyata K. Changes in anterior and posterior corneal curvatures in keratoconus. Ophthalmology. 2000;107:1328–1332. PubMed
Schlegel Z, Hoang-Xuan T, Gatinel D. Comparison of and correlation between anterior and posterior corneal elevation maps in normal eyes and keratoconus-suspect eyes. J Cataract Refract Surg. 2008;34:789–795. PubMed
Akhtar S, Bron AJ, Hayes AJ, Meek KM, Caterson B. Role of keratan sulphate (sulphated poly -N-acetyllactosamine repeats) in keratoconic cornea, histochemical, and ultrastructural analysis. Graefes Arch Clin Exp Ophthalmol. 2011;249:413–420. PubMed