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Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy
P. Liskova, NJ. Hafford-Tear, P. Skalicka, F. Malinka, J. Jedlickova, Ľ. Ďuďáková, N. Pontikos, AE. Davidson, S. Tuft
Language English Country England, Great Britain
Document type Journal Article
Grant support
MR/S031820/1
Medical Research Council - United Kingdom
NLK
Free Medical Journals
from 2008 to 1 year ago
Medline Complete (EBSCOhost)
from 2008-02-01 to 1 year ago
Wiley Free Content
from 2008 to 1 year ago
PubMed
35174971
DOI
10.1111/aos.15114
Knihovny.cz E-resources
- MeSH
- Astigmatism * MeSH
- Corneal Dystrophies, Hereditary * diagnosis genetics MeSH
- Child MeSH
- Adult MeSH
- Corneal Edema * MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Child, Preschool MeSH
- Cornea pathology MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Transcription Factors genetics MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Child, Preschool MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
PURPOSE: Posterior corneal vesicles (PCVs) have clinical features that are similar to posterior polymorphous corneal dystrophy (PPCD). To help determine whether there is a shared genetic basis, we screened 38 individuals with PCVs for changes in the three genes identified as causative for PPCD. METHODS: We prospectively recruited patients for this study. We examined all individuals clinically, with their first-degree relatives when available. We used a combination of Sanger and exome sequencing to screen regulatory regions of OVOL2 and GRHL2, and the entire ZEB1 coding sequence. RESULTS: The median age at examination was 37.5 years (range 4.7-84.0 years), 20 (53%) were male and in 19 (50%) the PCVs were unilateral. Most individuals were discharged to optometric review, but five had follow-up for a median of 12 years (range 5-13 years) with no evidence of progression. In cases with unilateral PCVs, there was statistically significant evidence that the change in the affected eye was associated with a lower endothelial cell density (p = 0.0003), greater central corneal thickness (p = 0.0277) and a steeper mean keratometry (p = 0.0034), but not with a higher keratometric astigmatism or a reduced LogMAR visual acuity. First-degree relatives of 13 individuals were available for examination, and in 3 (23%), PCVs were identified. No possibly pathogenic variants were identified in the PPCD-associated genes screened. CONCLUSION: We found no evidence that PCVs share the same genetic background as PPCD. In contrast to PPCD, we confirm that PCVs is a mild, non-progressive condition with no requirement for long-term review. However, subsequent cataract surgery can lead to corneal oedema.
Department of Computer Science Czech Technical University Prague Prague Czech Republic
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