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Treatment of Darier’s disease with oral magnesium: a case report

Darier’s disease, an autosomal dominant genodermatosis, arises from a mutation in the ATP2A2 gene that codes for sarco/endoplasmic reticulum Ca(2+)-ATPase in the endoplasmic reticulum and is characterized by greasy keratotic papules commonly found in seborrheic regions. Conventional treatments, incl...

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Autores principales: Oi-Yee Li, Heidi, Colantonio, Sophia, Kanigsberg, Nordau
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134490/
https://www.ncbi.nlm.nih.gov/pubmed/30214806
http://dx.doi.org/10.1177/2050313X18795071
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author Oi-Yee Li, Heidi
Colantonio, Sophia
Kanigsberg, Nordau
author_facet Oi-Yee Li, Heidi
Colantonio, Sophia
Kanigsberg, Nordau
author_sort Oi-Yee Li, Heidi
collection PubMed
description Darier’s disease, an autosomal dominant genodermatosis, arises from a mutation in the ATP2A2 gene that codes for sarco/endoplasmic reticulum Ca(2+)-ATPase in the endoplasmic reticulum and is characterized by greasy keratotic papules commonly found in seborrheic regions. Conventional treatments, including topical corticosteroids, antibiotics, antifungals and retinoids, often have limited efficacy. The present article reports the novel use of oral magnesium chloride supplementation (300 mg daily) in the treatment of Darier disease. After 5 years of limited improvement using conventional therapies, significant improvements in neck lesions were observed within 1 month of starting oral magnesium chloride. This suggests that oral magnesium chloride may be an effective therapeutic option for Darier disease, although further in vitro and clinical trials are necessary to evaluate its clinical efficacy.
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spelling pubmed-61344902018-09-13 Treatment of Darier’s disease with oral magnesium: a case report Oi-Yee Li, Heidi Colantonio, Sophia Kanigsberg, Nordau SAGE Open Med Case Rep JCMS Case Report Darier’s disease, an autosomal dominant genodermatosis, arises from a mutation in the ATP2A2 gene that codes for sarco/endoplasmic reticulum Ca(2+)-ATPase in the endoplasmic reticulum and is characterized by greasy keratotic papules commonly found in seborrheic regions. Conventional treatments, including topical corticosteroids, antibiotics, antifungals and retinoids, often have limited efficacy. The present article reports the novel use of oral magnesium chloride supplementation (300 mg daily) in the treatment of Darier disease. After 5 years of limited improvement using conventional therapies, significant improvements in neck lesions were observed within 1 month of starting oral magnesium chloride. This suggests that oral magnesium chloride may be an effective therapeutic option for Darier disease, although further in vitro and clinical trials are necessary to evaluate its clinical efficacy. SAGE Publications 2018-09-10 /pmc/articles/PMC6134490/ /pubmed/30214806 http://dx.doi.org/10.1177/2050313X18795071 Text en © The Author(s) 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle JCMS Case Report
Oi-Yee Li, Heidi
Colantonio, Sophia
Kanigsberg, Nordau
Treatment of Darier’s disease with oral magnesium: a case report
title Treatment of Darier’s disease with oral magnesium: a case report
title_full Treatment of Darier’s disease with oral magnesium: a case report
title_fullStr Treatment of Darier’s disease with oral magnesium: a case report
title_full_unstemmed Treatment of Darier’s disease with oral magnesium: a case report
title_short Treatment of Darier’s disease with oral magnesium: a case report
title_sort treatment of darier’s disease with oral magnesium: a case report
topic JCMS Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134490/
https://www.ncbi.nlm.nih.gov/pubmed/30214806
http://dx.doi.org/10.1177/2050313X18795071
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