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Dyskeratosis Congenita and Corneal Refractive Surgery

Dyskeratosis congenita is a syndrome of bone marrow failure secondary to unstable telomeres. It is characterized by a range of mucocutaneous diseases. Due to premature telomere shortening, these patients have limbal stem cell deficiency leading to poor regeneration and maintenance of the cornea. Man...

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Autores principales: Heiland, Madeline B., Moshirfar, Majid, Rosen, David B., Ronquillo, Yasmyne C., Hoopes, Phillip C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692790/
https://www.ncbi.nlm.nih.gov/pubmed/31313220
http://dx.doi.org/10.1007/s40123-019-0200-z
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author Heiland, Madeline B.
Moshirfar, Majid
Rosen, David B.
Ronquillo, Yasmyne C.
Hoopes, Phillip C.
author_facet Heiland, Madeline B.
Moshirfar, Majid
Rosen, David B.
Ronquillo, Yasmyne C.
Hoopes, Phillip C.
author_sort Heiland, Madeline B.
collection PubMed
description Dyskeratosis congenita is a syndrome of bone marrow failure secondary to unstable telomeres. It is characterized by a range of mucocutaneous diseases. Due to premature telomere shortening, these patients have limbal stem cell deficiency leading to poor regeneration and maintenance of the cornea. Many of these patients will require hematopoietic stem cell transplant in their lifetime, which poses a significant risk for acute and chronic graft-versus-host disease with and without ocular manifestations. We advise against elective corneal refractive surgery in patients with dyskeratosis congenita due to the compounded and long-term risks of delayed healing secondary to limbal stem cell deficiency and ocular complications of graft-versus-host disease post-allogeneic hematopoietic stem cell transplant.
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spelling pubmed-66927902019-08-26 Dyskeratosis Congenita and Corneal Refractive Surgery Heiland, Madeline B. Moshirfar, Majid Rosen, David B. Ronquillo, Yasmyne C. Hoopes, Phillip C. Ophthalmol Ther Commentary Dyskeratosis congenita is a syndrome of bone marrow failure secondary to unstable telomeres. It is characterized by a range of mucocutaneous diseases. Due to premature telomere shortening, these patients have limbal stem cell deficiency leading to poor regeneration and maintenance of the cornea. Many of these patients will require hematopoietic stem cell transplant in their lifetime, which poses a significant risk for acute and chronic graft-versus-host disease with and without ocular manifestations. We advise against elective corneal refractive surgery in patients with dyskeratosis congenita due to the compounded and long-term risks of delayed healing secondary to limbal stem cell deficiency and ocular complications of graft-versus-host disease post-allogeneic hematopoietic stem cell transplant. Springer Healthcare 2019-07-16 2019-09 /pmc/articles/PMC6692790/ /pubmed/31313220 http://dx.doi.org/10.1007/s40123-019-0200-z Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Commentary
Heiland, Madeline B.
Moshirfar, Majid
Rosen, David B.
Ronquillo, Yasmyne C.
Hoopes, Phillip C.
Dyskeratosis Congenita and Corneal Refractive Surgery
title Dyskeratosis Congenita and Corneal Refractive Surgery
title_full Dyskeratosis Congenita and Corneal Refractive Surgery
title_fullStr Dyskeratosis Congenita and Corneal Refractive Surgery
title_full_unstemmed Dyskeratosis Congenita and Corneal Refractive Surgery
title_short Dyskeratosis Congenita and Corneal Refractive Surgery
title_sort dyskeratosis congenita and corneal refractive surgery
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6692790/
https://www.ncbi.nlm.nih.gov/pubmed/31313220
http://dx.doi.org/10.1007/s40123-019-0200-z
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