Associated Papers
Beneath the surface: delineating the subtypes of Dowling-Degos disease.
Kumar S et al.
The British Journal of Dermatology, 2025
Galli-Galli Disease: A Comprehensive Literature Review.
Michelerio A et al.
Dermatopathology (basel, Switzerland), 2024
Atypical Disseminated Variant of Galli-Galli Disease: A Review of the Literature.
Yang A et al.
The American Journal of Dermatopathology, 2020
Updated review of genetic reticulate pigmentary disorders.
Zhang J et al.
The British Journal of Dermatology, 2017
Genome-wide linkage and exome sequencing analyses identify an initiation codon mutation of KRT5 in a unique Chinese family with generalized Dowling-Degos disease.
Li M et al.
The British Journal of Dermatology, 2016
[Galli-Galli disease. Clinical and histopathological investigation using a case series of 18 patients].
Hanneken S et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete, 2011
Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease.
Hanneken S et al.
The British Journal of Dermatology, 2010
Galli-Galli disease is an acantholytic variant of Dowling-Degos disease.
Sprecher E et al.
The British Journal of Dermatology, 2007
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