Results 51 to 60 of about 2,444 (225)

Telangiectasia macularis eruptiva perstans: More Than Skin Deep [PDF]

open access: yes, 2011
Systemic mastocytosis is a rare disease involving the infiltration and accumulation of active mast cells within any organ system. By far, the most common organ affected is the skin. Cutaneous manifestations of mastocytosis, including Urticaria Pigmentosa
Bokor, Winston B.   +4 more
core   +2 more sources

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

A Case of Familial Comedonal Darier's Disease [PDF]

open access: yes, 2011
Darier's disease is a genetic disorder of keratinization with autosomal dominant inheritance. Its appearance is usually in the form of greasy, crusted, keratotic yellow-brown papules and plaques found particularly on seborrheic areas of the body. However,
Aliağaoğlu   +19 more
core   +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

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders [PDF]

open access: yes, 2016
Personality is influenced by genetic and environmental factors1 and associated with mental health. However, the underlying genetic determinants are largely unknown.
A Okbay   +82 more
core   +3 more sources

Darier’s disease with epilepsy in an elderly patient after surgery for aortic dissection [PDF]

open access: yes, 2021
journal ...
Akiyama, Masashi   +4 more
core   +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

Clinical, histopathological and immunofluorescent study of vesicobullous lesions of skin [PDF]

open access: yes, 2019
Background: Vesiculobullous diseases have been the focus of intensive investigation in recent years. However, these disorders are still associated with substantial morbidity, considerable mortality and impaired quality of life.
Atla, Bhagyalakshmi   +5 more
core   +2 more sources

Linear Darier disease

open access: yesDermatology Online Journal, 2008
Darier disease is an uncommon genodermatosis characterized by verrucous papules in a seborrheic distribution. The linear form of this disease is rare and could result from genetic mosaicism in this autosomal dominant disorder. We report a case of linear Darier disease that involved the right lower limb with a zosteriform distribution.
Meziane, Mariame   +4 more
openaire   +4 more sources

Rare ocular manifestations in keratosis follicularis (Darier–White disease)

open access: yesIndian Journal of Ophthalmology, 2017
Keratosis follicularis (Darier's disease) is a rare (1 in 30,000–100,000) genetic autosomal-dominant predominantly dermatological disorder characterized by hyperkeratosis and acantholysis due to a defective calcium transport in the cells. Ocular findings,
Savitha H Kanakpur, Divya Upendra Caculo
doaj   +1 more source

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