Vesicular variant of Dowling-Degos disease
Author:
Affiliation:
1. Department of Dermatology, Venereology and Allergy; University Medical Center and Medical Faculty Mannheim; Heidelberg University; Theodor-Kutzer-Ufer 1-3 68167 Mannheim Germany
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.16906/fullpdf
Reference8 articles.
1. Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease;Hanneken;Br J Dermatol,2010
2. Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease;Betz;Am J Hum Genet,2006
3. Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease;Basmanav;Am J Hum Genet,2014
4. Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder;González-Villanueva;Br J Dermatol,2018
5. Mutations in γ-secretase subunit-encoding PSENEN underlie Dowling-Degos disease associated with acne inversa;Ralser;J Clin Invest,2017
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1. Reticulated Hyperpigmentation;Atlas of Pigmentary Skin Disorders;2023
2. Papules évocatrices de kératoses séborrhéiques au cours de la maladie de Dowling–Degos;Annales de Dermatologie et de Vénéréologie - FMC;2021-09
3. Comedonal Lesions on the Trunk and Proximal Extremities: Answer;The American Journal of Dermatopathology;2021-04
4. Dowling–Degos disease: A case report of a follicular variant;Journal of Dermatology and Dermatologic Surgery;2021
5. Dowling‐Degos disease: a review;International Journal of Dermatology;2020-12-23
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