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Fading Kayser–Fleischer ring revisited

Kayser-Fleischer (KF) ring, caused by deposition of excess copper in the Descemet membrane, is a characteristic ocular manifestation of Wilson disease (WD). Disappearance of KF rings following successful treatment of Wilson disease is typically a slow process that occurs over years. Herein, we descr...

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Detalles Bibliográficos
Autores principales: Sethi, Maansi, Madan, Siddharth, Beri, Sarita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982938/
https://www.ncbi.nlm.nih.gov/pubmed/35391817
http://dx.doi.org/10.4103/1319-4534.337854
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author Sethi, Maansi
Madan, Siddharth
Beri, Sarita
author_facet Sethi, Maansi
Madan, Siddharth
Beri, Sarita
author_sort Sethi, Maansi
collection PubMed
description Kayser-Fleischer (KF) ring, caused by deposition of excess copper in the Descemet membrane, is a characteristic ocular manifestation of Wilson disease (WD). Disappearance of KF rings following successful treatment of Wilson disease is typically a slow process that occurs over years. Herein, we describe a 19-year old girl who presented with neuropsychiatric manifestations and was found to have KF rings on slit lamp examination. Subsequent evaluation (brain imaging, liver function tests, serum ceruloplasmin and urinary copper studies) confirmed a diagnosis of Wilson disease with neurological and hepatic involvement. She was treated with d-penicillamine. She had remarkable fading of KF rings within a span of 6 months of copper-chelating therapy, which was also associated with significant improvement in her neurological symptoms. Though KF rings are a harbinger of neurological Wilson's, their disappearance does not always correlate with systemic improvement – an interesting finding in this case.
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spelling pubmed-89829382022-04-06 Fading Kayser–Fleischer ring revisited Sethi, Maansi Madan, Siddharth Beri, Sarita Saudi J Ophthalmol Case Report Kayser-Fleischer (KF) ring, caused by deposition of excess copper in the Descemet membrane, is a characteristic ocular manifestation of Wilson disease (WD). Disappearance of KF rings following successful treatment of Wilson disease is typically a slow process that occurs over years. Herein, we describe a 19-year old girl who presented with neuropsychiatric manifestations and was found to have KF rings on slit lamp examination. Subsequent evaluation (brain imaging, liver function tests, serum ceruloplasmin and urinary copper studies) confirmed a diagnosis of Wilson disease with neurological and hepatic involvement. She was treated with d-penicillamine. She had remarkable fading of KF rings within a span of 6 months of copper-chelating therapy, which was also associated with significant improvement in her neurological symptoms. Though KF rings are a harbinger of neurological Wilson's, their disappearance does not always correlate with systemic improvement – an interesting finding in this case. Wolters Kluwer - Medknow 2022-02-18 /pmc/articles/PMC8982938/ /pubmed/35391817 http://dx.doi.org/10.4103/1319-4534.337854 Text en Copyright: © 2022 Saudi Journal of Ophthalmology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Sethi, Maansi
Madan, Siddharth
Beri, Sarita
Fading Kayser–Fleischer ring revisited
title Fading Kayser–Fleischer ring revisited
title_full Fading Kayser–Fleischer ring revisited
title_fullStr Fading Kayser–Fleischer ring revisited
title_full_unstemmed Fading Kayser–Fleischer ring revisited
title_short Fading Kayser–Fleischer ring revisited
title_sort fading kayser–fleischer ring revisited
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982938/
https://www.ncbi.nlm.nih.gov/pubmed/35391817
http://dx.doi.org/10.4103/1319-4534.337854
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