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Fertility in Cystinosis

Cystinosis is a rare inheritable lysosomal storage disorder characterized by cystine accumulation throughout the body, chronic kidney disease necessitating renal replacement therapy mostly during adolescence, and multiple extra-renal complications. The majority of male cystinosis patients are infert...

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Detalles Bibliográficos
Autores principales: Reda, Ahmed, Veys, Koenraad, Besouw, Martine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700558/
https://www.ncbi.nlm.nih.gov/pubmed/34944047
http://dx.doi.org/10.3390/cells10123539
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author Reda, Ahmed
Veys, Koenraad
Besouw, Martine
author_facet Reda, Ahmed
Veys, Koenraad
Besouw, Martine
author_sort Reda, Ahmed
collection PubMed
description Cystinosis is a rare inheritable lysosomal storage disorder characterized by cystine accumulation throughout the body, chronic kidney disease necessitating renal replacement therapy mostly during adolescence, and multiple extra-renal complications. The majority of male cystinosis patients are infertile due to azoospermia, in contrast to female patients who are fertile. Over recent decades, the fertility status of male patients has evolved from a primary hypogonadism in the era before the systematic treatment with cysteamine to azoospermia in the majority of cysteamine-treated infantile cystinosis patients. In this review, we provide a state-of-the-art overview on the available clinical, histopathological, animal, and in vitro data. We summarize current insights on both cystinosis males and females, and their clinical implications including the potential effect of cysteamine on fertility. In addition, we identify the remaining challenges and areas for future research.
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spelling pubmed-87005582021-12-24 Fertility in Cystinosis Reda, Ahmed Veys, Koenraad Besouw, Martine Cells Review Cystinosis is a rare inheritable lysosomal storage disorder characterized by cystine accumulation throughout the body, chronic kidney disease necessitating renal replacement therapy mostly during adolescence, and multiple extra-renal complications. The majority of male cystinosis patients are infertile due to azoospermia, in contrast to female patients who are fertile. Over recent decades, the fertility status of male patients has evolved from a primary hypogonadism in the era before the systematic treatment with cysteamine to azoospermia in the majority of cysteamine-treated infantile cystinosis patients. In this review, we provide a state-of-the-art overview on the available clinical, histopathological, animal, and in vitro data. We summarize current insights on both cystinosis males and females, and their clinical implications including the potential effect of cysteamine on fertility. In addition, we identify the remaining challenges and areas for future research. MDPI 2021-12-15 /pmc/articles/PMC8700558/ /pubmed/34944047 http://dx.doi.org/10.3390/cells10123539 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Reda, Ahmed
Veys, Koenraad
Besouw, Martine
Fertility in Cystinosis
title Fertility in Cystinosis
title_full Fertility in Cystinosis
title_fullStr Fertility in Cystinosis
title_full_unstemmed Fertility in Cystinosis
title_short Fertility in Cystinosis
title_sort fertility in cystinosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8700558/
https://www.ncbi.nlm.nih.gov/pubmed/34944047
http://dx.doi.org/10.3390/cells10123539
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