Bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: Surgical challenges and the added value of intraoperative optical coherence tomography

This study aimed to describe the surgical challenges, management, and value of intraoperative optical coherence tomography in a case of a bilateral Descemet Stripping Automated Endothelial Keratoplasty corneal transplantation at 17 weeks of age for the treatment of severe posterior polymorphous corn...

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Detalles Bibliográficos
Autores principales: Muijzer, Marc B., Kroes, Hester Y., van Hasselt, Peter M., Wisse, Robert P. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8978779/
https://www.ncbi.nlm.nih.gov/pubmed/35387289
http://dx.doi.org/10.1002/ccr3.5637
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author Muijzer, Marc B.
Kroes, Hester Y.
van Hasselt, Peter M.
Wisse, Robert P. L.
author_facet Muijzer, Marc B.
Kroes, Hester Y.
van Hasselt, Peter M.
Wisse, Robert P. L.
author_sort Muijzer, Marc B.
collection PubMed
description This study aimed to describe the surgical challenges, management, and value of intraoperative optical coherence tomography in a case of a bilateral Descemet Stripping Automated Endothelial Keratoplasty corneal transplantation at 17 weeks of age for the treatment of severe posterior polymorphous corneal dystrophy resulting from a de novo mutation of the OVOL2‐gene.
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spelling pubmed-89787792022-04-05 Bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: Surgical challenges and the added value of intraoperative optical coherence tomography Muijzer, Marc B. Kroes, Hester Y. van Hasselt, Peter M. Wisse, Robert P. L. Clin Case Rep Case Reports This study aimed to describe the surgical challenges, management, and value of intraoperative optical coherence tomography in a case of a bilateral Descemet Stripping Automated Endothelial Keratoplasty corneal transplantation at 17 weeks of age for the treatment of severe posterior polymorphous corneal dystrophy resulting from a de novo mutation of the OVOL2‐gene. John Wiley and Sons Inc. 2022-04-04 /pmc/articles/PMC8978779/ /pubmed/35387289 http://dx.doi.org/10.1002/ccr3.5637 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Muijzer, Marc B.
Kroes, Hester Y.
van Hasselt, Peter M.
Wisse, Robert P. L.
Bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: Surgical challenges and the added value of intraoperative optical coherence tomography
title Bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: Surgical challenges and the added value of intraoperative optical coherence tomography
title_full Bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: Surgical challenges and the added value of intraoperative optical coherence tomography
title_fullStr Bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: Surgical challenges and the added value of intraoperative optical coherence tomography
title_full_unstemmed Bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: Surgical challenges and the added value of intraoperative optical coherence tomography
title_short Bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: Surgical challenges and the added value of intraoperative optical coherence tomography
title_sort bilateral posterior lamellar corneal transplant surgery in an infant of 17 weeks old: surgical challenges and the added value of intraoperative optical coherence tomography
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8978779/
https://www.ncbi.nlm.nih.gov/pubmed/35387289
http://dx.doi.org/10.1002/ccr3.5637
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