Cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review

Achini K Makuloluwa, Fatemeh Shams Tennent Institute of Ophthalmology, Gartnavel General Hospital, Glasgow, UK Abstract: Cystinosis is a rare, autosomal recessive disorder leading to defective transport of cystine out of lysosomes. Subsequent cystine crystal accumulation can occur in various tissu...

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Autores principales: Makuloluwa AK, Shams F
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2018
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Acceso en línea:https://doaj.org/article/eb7925af644b4eba9c65507aebaefd2d
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spelling oai:doaj.org-article:eb7925af644b4eba9c65507aebaefd2d2021-12-02T02:53:32ZCysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review1177-5483https://doaj.org/article/eb7925af644b4eba9c65507aebaefd2d2018-01-01T00:00:00Zhttps://www.dovepress.com/cysteamine-hydrochloride-eye-drop-solution-for-the-treatment-of-cornea-peer-reviewed-article-OPTHhttps://doaj.org/toc/1177-5483Achini K Makuloluwa, Fatemeh Shams Tennent Institute of Ophthalmology, Gartnavel General Hospital, Glasgow, UK Abstract: Cystinosis is a rare, autosomal recessive disorder leading to defective transport of cystine out of lysosomes. Subsequent cystine crystal accumulation can occur in various tissues, including the ocular surface. This review explores the efficacy of cysteamine hydrochloride eye drops in the treatment of corneal cystine crystal accumulation and its safety profile. Keywords: cysteine, CTNS gene, cystaran, cystadropsMakuloluwa AKShams FDove Medical PressarticleOphthalmologyRE1-994ENClinical Ophthalmology, Vol Volume 12, Pp 227-236 (2018)
institution DOAJ
collection DOAJ
language EN
topic Ophthalmology
RE1-994
spellingShingle Ophthalmology
RE1-994
Makuloluwa AK
Shams F
Cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review
description Achini K Makuloluwa, Fatemeh Shams Tennent Institute of Ophthalmology, Gartnavel General Hospital, Glasgow, UK Abstract: Cystinosis is a rare, autosomal recessive disorder leading to defective transport of cystine out of lysosomes. Subsequent cystine crystal accumulation can occur in various tissues, including the ocular surface. This review explores the efficacy of cysteamine hydrochloride eye drops in the treatment of corneal cystine crystal accumulation and its safety profile. Keywords: cysteine, CTNS gene, cystaran, cystadrops
format article
author Makuloluwa AK
Shams F
author_facet Makuloluwa AK
Shams F
author_sort Makuloluwa AK
title Cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review
title_short Cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review
title_full Cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review
title_fullStr Cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review
title_full_unstemmed Cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review
title_sort cysteamine hydrochloride eye drop solution for the treatment of corneal cystine crystal deposits in patients with cystinosis: an evidence-based review
publisher Dove Medical Press
publishDate 2018
url https://doaj.org/article/eb7925af644b4eba9c65507aebaefd2d
work_keys_str_mv AT makuloluwaak cysteaminehydrochlorideeyedropsolutionforthetreatmentofcornealcystinecrystaldepositsinpatientswithcystinosisanevidencebasedreview
AT shamsf cysteaminehydrochlorideeyedropsolutionforthetreatmentofcornealcystinecrystaldepositsinpatientswithcystinosisanevidencebasedreview
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