Galli-Galli disease is an acantholytic variant of Dowling-Degos disease: Additional genetic evidence in a German family
Author:
Publisher
Elsevier BV
Subject
Dermatology
Reference5 articles.
1. Acanthosis nigricans;Dowling;Proc R Soc Med,1938
2. Dowling-Degos disease (reticulate pigmented anomaly of the flexures) is an autosomal dominant condition;Crovato;Br J Dermatol,1983
3. Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos disease;Betz;Am J Hum Genet,2006
4. Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease;Hanneken;Br J Dermatol,2010
5. 1,24-Dihydroxyvitamin D (tacalcitol) prevents skin T-cell infiltration;Yamanaka;Br J Dermatol,2010
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1. Inherited Acantholytic Disorders;Rook's Textbook of Dermatology;2024-02-20
2. Galli–Galli Disease: A Comprehensive Literature Review;Dermatopathology;2024-02-07
3. A loss‐of‐function NCSTN mutation associated with familial Dowling Degos disease and hidradenitis suppurativa;Experimental Dermatology;2023-09-04
4. Vielfältige Klinik, differenzierte Therapie;Deutsche Dermatologie;2022-10
5. Exacerbation of Galli-Galli Disease Following Dialysis Treatment: A Case Report and Review of Aggravating Factors;Cureus;2021-06-02
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