Results 21 to 30 of about 831 (131)

Unilateral and pruritic papules: segmental Darier-White disease [PDF]

Dermatology Online Journal, 2014
Darier-White disease is an uncommon disorder, which presents in a localized pattern in about 10% of patients, usually without nail, mucosa, or acral involvement. Type-1 is the most common of the segmental Darier-White disease types: papules have unilateral distribution along Blaschko lines.
Puente, Nieves, Nieto, Olga, Tardino, Juan C, Borbujo, Jesus   +3 more
openaire   +5 more sources

Darier′s disease - Oral, general and histopathological features in a 7 year old child

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2016
Darier′s disease, also known as keratosis follicularis, is a rare autosomal dominant genodermatosis, manifesting clinically as hyperkeratotic, firm papule that predominates in the seborrheic areas and flexures with accompanying nail abnormalities.
Sreedevi Dharman, Muthukrishnan Arvind
doaj   +1 more source

Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort

Advanced Genetics, 2023
Interstitial cystitis/bladder pain syndrome (IC/BPS) is a chronic pain disorder causing symptoms of urinary frequency, urgency, and bladder discomfort or pain.
Elicia Estrella, Shira Rockowitz, Marielle Thorne, Pressley Smith, Jeanette Petit, Veronica Zehnder, Richard N. Yu, Stuart Bauer, Charles Berde, Pankaj B. Agrawal, Alan H. Beggs, Ali G. Gharavi, Louis Kunkel, Catherine A. Brownstein   +13 more
doaj   +1 more source

Unilateral Darier’s disease – case report

Przegląd 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, Karolina Rajkowska-Strojs, Katarzyna Chrzanowska   +2 more
doaj   +1 more source

Inframammary Dermatitis: A Case of Localized Late-Onset Darier’s Disease

Case Reports in Dermatology, 2016
Darier’s disease (DD) is an autosomal dominant inherited genodermatosis which is often under- or misdiagnosed. In the majority of cases, the disease manifests in adolescents or young adults with small brownish-yellow, warty, hyperkeratotic papules in ...
Dennis Linder, Elena Marinello, Pietro Maria Donisi, Roberto Salmaso, Edoardo Zattra, Anna Zampetti   +5 more
doaj   +1 more source

Tight junctions in Hailey-Hailey and Darier’s diseases

Dermatology Reports, 2009
Hailey-Hailey disease (HHD) and Darier’s disease (DD) are caused by mutations in Ca2+-ATPases with the end result of desmosomal disruption and suprabasal acantholysis.
Laura Raiko, Pekka Leinonen, Päivi Hägg, Juha Peltonen, Aarne Oikarinen, Sirkku Peltonen   +5 more
doaj   +1 more source

Basal Cell Carcinoma in Type 2 Segmental Darier's Disease

Journal of Skin Cancer, 2012
Background. Darier's disease (DD), also known as Keratosis Follicularis or Darier-White disease, is a rare disorder of keratinization. DD can present as a generalized autosomal dominant condition as well as a localized or segmental postzygotic condition (
Lynne Robertson, Maxwell B. Sauder
doaj   +1 more source

Darier disease—A review highlighting new insights from the Darier Disease International Task Force

Journal of the European Academy of Dermatology and Venereology, EarlyView.
This review provides a global, clinically focused overview of DD, detailing cutaneous and extracutaneous manifestations, disease classification and severity scoring. It emphasizes early recognition, multidisciplinary management and practical guidance for dermatologists to apply evidence‐based care in diverse skin phototypes. Abstract Darier disease (DD)
Sofia Labbouz, Alain Hovnanian, Grace Xiong, Dedee Frances Murrell, Simon M. Mueller, Khaled Ezzedine, Nessa Aghazadeh Mohandesi, Ahmed Salem Aldhaheri, Nissim Asayag, Eulalia Baselga, Chen Nadler, Keith Choate, Chia‐Yu Chu, John Robert Edminister, Emmanuella Guenova, Melis Gönülal, Antoni Gostynski, Ankan Gupta, Lalit Kumar Gupta, Juliette Mazereeuw‐Hautier, Wolfram Hoetzenecker, Peter Itin, Marek Jankowski, Akiharu Kubo, Haur Yueh Lee, Julia Scott Lehman, Anfisa Lepekhova, Márta Medvecz, Jemima E. Mellerio, Verena Moosbrugger‐Martinz, Amy S. Paller, Dóra Plázár, Amadeu José Rodrigues Queiróz, Josep Riera‐Monroig, Ralph Rosa, Matthias Schmuth, Maella Severino Freire, Itzhak Shabat, Jonathan Shapiro, Cory L. Simpson, Diego Soto‐García, Alexander J. Stratigos, Gianluca Abel Tadini, Takuya Takeichi, Kaushal K. Verma, Jakob D. Wikström, Alexander Zink, Michael Ziv, Alexander Navarini, Roni Pircha Dodiuk‐Gad   +49 more
wiley   +1 more source

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

Case 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, Poonkiat Suchonwanit   +1 more
doaj   +1 more source

A Telangiectasia Macularis Eruptiva Perstans in a Child: A Rare Vascular Phenotype of Cutaneous Mastocytosis

Case Reports in Pediatrics, Volume 2026, Issue 1, 2026.
Telangiectasia macularis eruptiva perstans (TMEP) is a rare vascular phenotype of cutaneous mastocytosis predominantly reported in adults; pediatric cases are exceptional and are particularly difficult to recognize in darker skin phototypes. We report the case of a 4‐year‐old girl who presented with subtle brown macules and faint telangiectasias, in ...
Bouchra Baghad, Meriem Takiddine, Farida Marnissi, Soumiya Chiheb, Nikhat Kaura   +4 more
wiley   +1 more source