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Multimodal imaging in autosomal dominant Wolfram syndrome and long-term follow-up of laminations of the outer plexiform layer

Eye (2024)Cite this article

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In this case report, all data generated or analyzed are included.

References

  1. Hull S, Vincent AL. Lamination of the outer plexiform layer in dominant Wolfram disease. Investig Ophthalmol Vis Sci. 2022;63:513–A0090.

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  2. Majander A, Bitner-Glindzicz M, Chan CM, Duncan HJ, Chinnery PF, Subash M, et al. Lamination of the outer plexiform layer in optic atrophy caused by dominant WFS1 Mutations. Ophthalmology. 2016;123:1624–6.

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Funding

This research received support from the National Institute for Health and Care Research (NIHR) through the grant: BRC4 Gene and Cell Therapy.

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Authors and Affiliations

  1. Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK

    Peter Kiraly, Felix F. Reichel & M. Dominik Fischer

  2. Nuffield Laboratory of Ophthalmology, University of Oxford, Oxford, UK

    Peter Kiraly, Felix F. Reichel & M. Dominik Fischer

  3. Centre for Ophthalmology, University Hospital Tubingen, Tubingen, Germany

    Felix F. Reichel & M. Dominik Fischer

Authors
  1. Peter Kiraly
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  2. Felix F. Reichel
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  3. M. Dominik Fischer
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Contributions

Design and concept by PK and MDF; manuscript drafting by PK; manuscript review and editing by MDF, PK, and FFR; visualization by PK; project administration by PK.

Corresponding author

Correspondence to Peter Kiraly.

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Competing interests

The authors declare no competing interests.

Ethical approval

Written informed consent for publication was secured from the patient. Given that this case report presents observational clinical data, ethics approval was not required, provided that patient consent was obtained and confidentiality was maintained.

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Kiraly, P., Reichel, F.F. & Fischer, M.D. Multimodal imaging in autosomal dominant Wolfram syndrome and long-term follow-up of laminations of the outer plexiform layer. Eye (2024). https://doi.org/10.1038/s41433-024-03114-0

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  • DOI: https://doi.org/10.1038/s41433-024-03114-0

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