Results 31 to 40 of about 1,614 (134)

Vesiculobullous variant of Darier’s disease with flexural freckle-like macules: A rarer presentation of a rare disease

open access: yesAnnals of Medical Science and Research, 2023
The bullous variant of Darier’s disease is a rare subtype and is often clinically and histologically similar to Hailey–Hailey disease (HHD). We report a case on similar lines of Darier’s disease presenting with dirty warty papules and freckle-like ...
Subhamoy Neogi   +3 more
doaj   +1 more source

Darier White disease

open access: yesNepal Journal of Dermatology, Venereology & Leprology, 2012
Darier’s disease was described inependently by Darier and White in 1989 AD. Reported prevalence varies from 1/100,000 in Denmark to 1 in 30- 35,000 in northern England and Scotland.1 Darier’s disease has been reported from other parts of the world ...
A Amatya   +5 more
doaj   +3 more sources

Unilateral Darier’s disease – case report

open access: yesPrzegląd Dermatologiczny, 2017
Introduction . Darier’s disease (dyskeratosis follicularis, keratosis follicularis, Darier-White disease, Darier disease) is a rare genodermatosis inherited in autosomal dominant manner, caused by a mutation in the ATP2A2 gene located on chromosome 12 ...
Jolanta Węgłowska   +2 more
doaj   +1 more source

Darier-White disease: A rare genetic disorder [PDF]

open access: yesJDVI (Journal of General Procedural Dermatology & Venereology Indonesia), 2018
Background: The clinical manifestation of Darier-White disease, an autosomal dominant genodermatosis, are greasy hyperkeratotic papules in seborrheic regions with nail abnormalities and mucous membrane changes due to a defective sarcoendoplasmic calcium ...
Cara Lynn Marie N. Chia   +3 more
doaj   +1 more source

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

open access: yesDermatology 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   +1 more source

Type I Segmental Darier’s Disease: Successful Treatment with Oral Acitretin- A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2023
Unilateral type I segmental Darier’s Disease (DD) is a rare variant of DD. It is characterised by eruptions which are erythematous and keratotic papules.
Shanmugam Reddy Praveen Kumar   +3 more
doaj   +1 more source

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

open access: yesJournal 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   +1 more source

Dermoscopy of Localized Darier's Disease in Fitzpatrick Type IV Skin.

open access: diamondIndian Dermatol Online J, 2020
Adya KA, Inamadar AC, Palit A.
europepmc   +2 more sources

Cooccurrence of Darier’s Disease and Epilepsy: A Pediatric Case Report and Review of the Literature

open access: yesCase Reports in Pediatrics, 2014
Darier’s disease is a skin disorder characterized by multiple eruptions of hyperkeratosis or crusted papules at seborrheic areas with histologic acantholysis and dyskeratosis. It is caused by mutations in a single gene, being ATP2A2 and that is expressed
Tamer Celik   +5 more
doaj   +1 more source

Late onset Darier’s Disease with Palmoplantar Keratoderma: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research
Darier’s disease is an infrequently encountered autosomal dominant condition characterised by complete penetrance but variable expression. It is characterised by abnormal keratinisation and epidermal adhesion deficiency, clinically presenting as greasy ...
Noshin N Abdu, Shaheela Backar
doaj   +1 more source

Home - About - Disclaimer - Privacy