Results 31 to 40 of about 1,614 (134)
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
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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
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Unilateral Darier’s disease – case report
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
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Darier-White disease: A rare genetic disorder [PDF]
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
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Dermoscopy: a useful auxiliary tool in the diagnosis of type 1 segmental Darier’s disease
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
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Type I Segmental Darier’s Disease: Successful Treatment with Oral Acitretin- A Case Report [PDF]
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
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Spectrum of features in Darier’s disease: A case report with emphasis on differential diagnosis
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
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Dermoscopy of Localized Darier's Disease in Fitzpatrick Type IV Skin.
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
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
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Late onset Darier’s Disease with Palmoplantar Keratoderma: A Case Report [PDF]
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
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