Management of familial benign chronic pemphigus

Benign familial chronic pemphigus or Hailey–Hailey disease is caused by an autosomal dominant mutation in the ATP2C1 gene leading to suprabasilar acantholysis. The disease most commonly affects intertriginous areas symmetrically. The chronic nature of the disease and multiple recurrences make the di...

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Detalles Bibliográficos
Autores principales: Arora, Harleen, Bray, Fleta N, Cervantes, Jessica, Falto Aizpurua, Leyre A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027951/
https://www.ncbi.nlm.nih.gov/pubmed/27695354
http://dx.doi.org/10.2147/CCID.S89483

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027951/
https://www.ncbi.nlm.nih.gov/pubmed/27695354
http://dx.doi.org/10.2147/CCID.S89483

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