Vesicular Darier’s disease: a case report and review of the English literature of a rare disease variant

Darier’s disease is an autosomal dominant inherited skin disorder resulting from mutations in the ATP2A2 gene, which encodes SERCA2, an endoplasmic reticulum calcium ATPase. Darier’s disease classically manifests as confluent hyperkeratotic brown-to-red papules that manifest and follow a seborrheic...

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Detalles Bibliográficos
Autores principales: Mourad, Ahmed, Kurwa, Habib A, Haber, Richard M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
JCMS Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467227/
https://www.ncbi.nlm.nih.gov/pubmed/37654551
http://dx.doi.org/10.1177/2050313X231195467

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467227/
https://www.ncbi.nlm.nih.gov/pubmed/37654551
http://dx.doi.org/10.1177/2050313X231195467

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