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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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| Publicado en: | SAGE Open Med Case Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
SAGE Publications
2018
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6134490/ https://ncbi.nlm.nih.gov/pubmed/30214806 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050313X18795071 |
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