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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Detalles Bibliográficos
Autores principales: Oi-Yee Li, Heidi, Colantonio, Sophia, Kanigsberg, Nordau
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
JCMS Case Report
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

Internet

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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