Results 31 to 40 of about 10,294,639 (233)
Naltrexone, a therapeutic alternative in Darier disease
Darier disease is a clinically variable rare disease with autosomal dominant inheritance caused by mutations in ATP2A2 gene. It affects skin, mucous membranes, and nails.
Dennise L. Smith-Pellegrin +5 more
doaj +1 more source
Management of Darier disease: A review of the literature and update.
Darier disease (DD) is a rare type of inherited keratinizing disorder with no definitive therapeutic approach. The objective of this study is to provide a detailed literature review of all the available treatment modalities of Darier disease, including ...
R. Haber, Nicole Dib
semanticscholar +1 more source
Vertebral sarcoidosis with associated Darier-Roussy disease manifesting as acute back pain
Introduction: Sarcoidosis is a systemic granulomatous disease of unknown etiology, with a heterogenous clinical manifestation, progression, and prognosis.
Mohamad Syafeeq Faeez Md Noh +5 more
doaj +1 more source
Darier disease (DD) and Hailey‐Hailey disease (HHD) are rare disorders caused by mutations in the ATPase, Sarcoplasmic/Endoplasmic Reticulum Ca2+ Transporting 2 (ATP2A2) and ATPase Ca2+ Transporting Type 2C, Member 1 (ATP2C1) gene, respectively, which ...
H. Stanisz +5 more
semanticscholar +1 more source
Darier-White Disease with Sensorineural Hearing Loss – A Case Report
Darier-White disease (keratosis follicularis) is a rare autosomal dominant genodermatosis characterized by hyperkeratotic papules and plaques in seborrheic areas, often presenting with nail abnormalities and occasionally mucous membrane changes ...
E. B. Henshaw +2 more
doaj +2 more sources
We present a 58-year-old woman with bipolardisorder and with a longstanding history of yellowbrown,hyperkeratotic papules in a seborrheicdistribution and nail changes. Her father andpaternal grandmother had similar eruptions and alsohad psychiatric disease. Histopathologic examinationshowed acantholysis and dyskeratosis, which wasconsistent with Darier-
Christman, Mitalee P +5 more
openaire +4 more sources
Impaired calcium signalling and neuropsychiatric disorders in Darier disease: An exploratory review
Darier (Darier‐White) disease (DD) is an autosomal dominant skin disorder caused by pathogenic mutations in the ATP2A2 gene which encodes a calcium ATPase in the sarco‐endoplasmic reticulum (SERCA2). Defects in the SERCA2 protein lead to an impairment of
Austin B. Ambur +3 more
semanticscholar +1 more source
Darier disease, hypertrophic / vegetating type
Background A hypertrophic / vegetating variant of Darier disease causing massive verruciform genital tumors is exceedingly rare. Case presentation A woman in her late 50s underwent wide resection of vulva and inguinal skin due to massive verruciform ...
Caroline Passos Cardoso +4 more
doaj +1 more source
Dowling-Degos Disease: Case Report and Review of the Literature [PDF]
Dowling-Degos disease (DDD) is an unusual pigmentary disorder usually caused by mutations in keratin 5. A 44-year-old woman in good general health presented due to the recent appearance of numerous pigmented macules on her axillary and anogenital skin. A
Baran, Wojciech +3 more
core +1 more source
Darier′s disease in gastric malignancy: An unusual paraneoplastic phenomenon
Darier′s disease is an autosomal dominant genodermatosis resulting from ATP2A2 gene mutation. A 62-year-old male presented at our outpatient (OPD) with sudden-onset numerous dirty, warty papules over the head, neck, and back since 2 months ...
Anusree Gangopadhyay +5 more
doaj +1 more source

