Literature DB >> 25081284

Macular corneal dystrophy and associated corneal thinning.

L Dudakova1, M Palos2, M Svobodova2, J Bydzovsky2, L Huna2, K Jirsova1, A J Hardcastle3, S J Tuft4, P Liskova5.   

Abstract

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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Year:  2014        PMID: 25081284      PMCID: PMC4194335          DOI: 10.1038/eye.2014.164

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN: 0950-222X            Impact factor:   3.775


  22 in total

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2.  Keratoconus in 18 pairs of twins.

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3.  Study of p.N247S KERA mutation in a British family with cornea plana.

Authors:  Petra Liskova; Pirro G Hysi; Denise Williams; John R Ainsworth; Sunil Shah; Albert de la Chapelle; Stephen J Tuft; Shomi S Bhattacharya
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4.  Comparison of and correlation between anterior and posterior corneal elevation maps in normal eyes and keratoconus-suspect eyes.

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6.  Keratoconus associated with corneal macular dystrophy: in vivo confocal microscopic evaluation.

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9.  Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.

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10.  Keratoconus associated with other corneal dystrophies.

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Journal:  Cornea       Date:  2009-02       Impact factor: 2.651

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  6 in total

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2.  Transcriptome from opaque cornea of Fanconi anemia patient uncovers fibrosis and two connected players.

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3.  Evaluation of the Genetic Variation Spectrum Related to Corneal Dystrophy in a Large Cohort.

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4.  Detailed corneal and genetic characteristics of a pediatric patient with macular corneal dystrophy - case report.

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5.  Comparative Study of Anterior Eye Segment Measurements with Spectral Swept-Source and Time-Domain Optical Coherence Tomography in Eyes with Corneal Dystrophies.

Authors:  Anna K Nowinska; Sławomir J Teper; Dominika A Janiszewska; Anita Lyssek-Boron; Dariusz Dobrowolski; Robert Koprowski; Edward Wylegala
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6.  Molecular analysis of the CHST6 gene in Korean patients with macular corneal dystrophy: Identification of three novel mutations.

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  6 in total

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