Results 1 to 10 of about 1,447 (168)

Dermoscopy: a useful auxiliary tool in the diagnosis of type 1 segmental Darier’s disease [PDF]

open access: diamondDermatology Practical & Conceptual, 2016
Type 1 segmental Darier’s disease is a blaschkolinear variant of Darier’s disease resulting from a postzygotic mosaicism. Since it usually lacks diagnostic clues typical of the generalized form, including positive family history of the disease, nail and ...
Enzo Errichetti   +3 more
doaj   +7 more sources

Spectrum of features in Darier’s disease: A case report with emphasis on differential diagnosis [PDF]

open access: bronzeJournal of Oral Biology and Craniofacial Research, 2019
Oral genodermatoses includes a spectrum of inherited dermatological disorders with varying oral mucosal manifestations. Darier’s disease is an autosomal dominant disorder with defect in desmosomal attachment.
Shwetha V   +6 more
doaj   +4 more sources

Unmet Needs in Darier’s Disease from a Patient’s Perspective: Lessons Learnt from the German Registry [PDF]

open access: goldActa Dermato-Venereologica
The MDHHgermany registry was initiated to characterize the “real-life” situation of affected individuals with Darier’s disease (DD; Morbus Darier, MD) and Hailey-Hailey disease (HH), including their treatment and healthcare.
Danielle Rogner   +4 more
doaj   +4 more sources

Exacerbation of Darier’s disease with COVID-19 [PDF]

open access: goldJAAD Case Reports, 2022
Rachel Dykes, DO   +3 more
doaj   +3 more sources

Segmental Darier’s disease: A case report [PDF]

open access: yesSAGE Open Medical Case Reports, 2023
Segmental Darier’s disease is an uncommon subtype of Darier’s genodermatosis, resulting from a mutation in the ATPase type 2 during early embryogenesis.
Elena Pastukhova, Lauren LaBerge
doaj   +2 more sources

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

open access: yesSAGE Open Medical Case Reports, 2023
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.
Ahmed Mourad   +2 more
doaj   +2 more sources

Scalp Cobblestoning in Darier’s Disease [PDF]

open access: diamondIndian Dermatology Online Journal
Aravind Sivakumar   +3 more
doaj   +3 more sources

The association between Darier’s disease and schizophrenia : a case report [PDF]

open access: yesEuropean Psychiatry, 2023
Introduction Darier’s disease, also known as Darier-White disease or keratosis follicularis, is a rare autosomal dominant genodermatosis. Clinical experience has long suggested an association between neuropsychiatric abnormalities and Darier’s disease ...
M. Abdelkefi   +5 more
doaj   +2 more sources

Darier’s Disease: Report of a Case with Facial Involvement [PDF]

open access: goldCase Reports in Dermatology, 2019
Darier’s disease is a relatively rare autosomal dominant genodermatosis with a defect in the desmosomal attachment due to a mutation in the ATP2A2 gene.
Chaninan Kositkuljorn   +1 more
doaj   +2 more sources

Darier’s Disease Flare following COVID-19 Vaccine [PDF]

open access: goldCase Reports in Dermatology, 2021
Darier’s disease is a rare genodermatosis characterized clinically by dyskeratotic papules in the seborrheic and intertriginous areas and nail abnormalities. Dyskeratosis and acantholysis are typical histological findings.
Mette Vestergaard Elbæk   +2 more
doaj   +2 more sources

Home - About - Disclaimer - Privacy