| Literature DB >> 29865954 |
Kaien Gu1, Shane Silver1.
Abstract
Hailey-Hailey disease, or benign familial pemphigus, is a rare blistering disease originally described in 1939. The disease is due to an autosomal dominant mutation in the ATP2C1 gene on chromosome 3, which encodes for an adenosine triphosphate-dependent calcium pump in the Golgi apparatus whose function is to maintain intercellular calcium homeostasis. Common treatments for Hailey-Hailey disease involve calcineurin inhibitors, topical corticosteroids, topical or systemic antibiotics, topical antifungals, ablative lasers, or botulin toxin. In this case report, we highlight a unique case of Hailey-Hailey disease that was resistant to many conventional therapies and ultimately managed with oral magnesium citrate and high-dose vitamin D3.Entities:
Keywords: Hailey-Hailey disease; benign familial pemphigus; vitamin D
Mesh:
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Year: 2018 PMID: 29865954 DOI: 10.1177/1203475418756377
Source DB: PubMed Journal: J Cutan Med Surg ISSN: 1203-4754 Impact factor: 2.092