Vanita Berry
Multimorbidity due to novel pathogenic variants in theWFS1/RP1/NOD2genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn’s disease in a British family
Berry, Vanita; Ionides, Alexander; Georgiou, Michalis; Quinlan, Roy A; Michaelides, Michel
Authors
Alexander Ionides
Michalis Georgiou
Roy Quinlan r.a.quinlan@durham.ac.uk
Emeritus Professor
Michel Michaelides
Abstract
Background A five generation family has been analysed by whole exome sequencing (WES) for genetic associations with the multimorbidities of congenital cataract (CC), retinitis pigmentosa (RP) and Crohn’s disease (CD). Methods WES was performed for unaffected and affected individuals within the family pedigree followed by bioinformatic analyses of these data to identify disease-causing variants with damaging pathogenicity scores. Results A novel pathogenic missense variant in WFS1: c.1897G>C; p.V633L, a novel pathogenic nonsense variant in RP1: c.6344T>G; p.L2115* and a predicted pathogenic missense variant in NOD2: c.2104C>T; p.R702W are reported. The three variants cosegregated with the phenotypic combinations of autosomal dominant CC, RP and CD within individual family members. Conclusions Here, we report multimorbidity in a family pedigree listed on a CC register, which broadens the spectrum of potential cataract associated genes to include both RP1 and NOD2.
Citation
Berry, V., Ionides, A., Georgiou, M., Quinlan, R. A., & Michaelides, M. (2023). Multimorbidity due to novel pathogenic variants in theWFS1/RP1/NOD2genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn’s disease in a British family. BMJ Open Ophthalmology, 8(1), Article e001252. https://doi.org/10.1136/bmjophth-2023-001252
Journal Article Type | Article |
---|---|
Acceptance Date | Jun 8, 2023 |
Online Publication Date | Jul 14, 2023 |
Publication Date | 2023 |
Deposit Date | Jul 17, 2023 |
Publicly Available Date | Aug 1, 2023 |
Journal | BMJ Open Ophthalmology |
Electronic ISSN | 2397-3269 |
Publisher | BMJ Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 8 |
Issue | 1 |
Article Number | e001252 |
DOI | https://doi.org/10.1136/bmjophth-2023-001252 |
Public URL | https://durham-repository.worktribe.com/output/1169998 |
Files
Published Journal Article
(570 Kb)
PDF
Licence
http://creativecommons.org/licenses/by/4.0/
Publisher Licence URL
http://creativecommons.org/licenses/by/4.0/
Copyright Statement
© Author(s) (or their
employer(s)) 2023. Re-use
permitted under CC BY.
Published by BMJ.
You might also like
A novel frameshift variant in BCOR causes congenital nuclear cataract
(2024)
Journal Article
Downloadable Citations
About Durham Research Online (DRO)
Administrator e-mail: dro.admin@durham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search