Hailey–Hailey disease is a rare blistering dermatosis first described in 1939 by the brothers
Howard and Hugh Hailey. Its incidence is estimated at 1/50,000. The inheritance is …

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 …

The autosomal‐dominant genodermatoses Darier disease and Hailey‐Hailey disease
present special challenges to dermatologists. Despite their similar pathogenesis featuring …

NICE has accredited the process used by the British Association of Dermatologists to
produce clinical guidelines. The renewed accreditation is valid until 31 May 2021 and …

Importance Hailey-Hailey disease (HHD) is a rare, autosomal-dominant acantholytic
dermatosis characterized clinically by development of recurrent blisters and erosions in …

Abstract Background Patients with Hailey-Hailey and Darier diseases present with disabling
inflammatory lesions located in large skin folds, which are often exacerbated or induced by …

Hailey–Hailey disease (HHD) is an autosomal dominant genodermatosis and the defective
gene in HHD is ATP2C1, which encodes secretory pathway Ca2+/Mn2+ ATPase type 1 …

Описаны современные представления о предрасполагающих факторах, особенностях
гистологических и генетических изменений, роли кодирующего мутантного гена …

Zusammenfassung Die autosomal‐dominanten Genodermatosen Morbus Darier und
Morbus Hailey‐Hailey stellen Dermatologen vor besondere Herausforderungen. Trotz …

The article describes modern views on predisposing factors, histological and genetic
changes, the role of ATP2C1 encoding a mutant gene, localized on chromosome 3 in the …