Dowling–Degos disease (DDD) is a rare autosomal dominant condition characterized by multiple, small, round pigmented macules usually arranged in reticular pattern, chiefly distributed in axillae and groins. Here we are reporting three atypical cases of DDD in a family. They had hypopigmented macules with typical features of DDD indicating generalized DDD. Histopathology confirmed the diagnosis. We present these three cases to stress the existence of generalized DDD phenotype in the Indian population
are rare genodermatosis inherited as an auto-somal dominant trait with variable pene-trance. They ar...
AbstractDyschromatosis universalis hereditaria (DUH) is a rare disease that is inherited both in aut...
Galli-Galli disease is a rare acantholytic variant of Dowling-Degos disease, with few cases reported...
Dowling Degos disease is a rare condition inherited as autosomal dominant trait characterized by num...
Dowling–Degos disease (DDD) is a rare genodermatosis with autosomal dominant inheritance. It is char...
Dowling-Degos Disease (DDD), is a rare, autosomal dominantly inherited pigmentation disorder. It is...
Dowling-Degos disease (DDD) is an autosomal dominant genodermatosis and this disease is a geneticall...
Dowling–Degos disease (DDD) and reticulate acropigmentation of Kitamura (RAK) are rare genodermatose...
Dowling-Degos disease (DDD) is an unusual pigmentary disorder usually caused by mutations in keratin...
Dyschromatosis universalis hereditaria (DUH) is a rare pigmentary disorder characterized by the pres...
Herein we report a rare case of classical Dowling-Degos disease (DDD) in a Taiwanese woman. A 23-yea...
A doença de Dowling-Degos é uma genodermatose rara que consiste numa desordem pigmentar reticulada. ...
Reticulate acral and flexural pigmentary disorders are a rare group of pigmentary genodermatoses. We...
Galli-Galli disease is a rare acantholytic variant of Dowling-Degos disease, with few cases reported...
6N/AreservedmixedPiccolo V, Corneli P, Russo T, Danielsson M, Zalaudek I, Argenziano G.Piccolo, V; C...
are rare genodermatosis inherited as an auto-somal dominant trait with variable pene-trance. They ar...
AbstractDyschromatosis universalis hereditaria (DUH) is a rare disease that is inherited both in aut...
Galli-Galli disease is a rare acantholytic variant of Dowling-Degos disease, with few cases reported...
Dowling Degos disease is a rare condition inherited as autosomal dominant trait characterized by num...
Dowling–Degos disease (DDD) is a rare genodermatosis with autosomal dominant inheritance. It is char...
Dowling-Degos Disease (DDD), is a rare, autosomal dominantly inherited pigmentation disorder. It is...
Dowling-Degos disease (DDD) is an autosomal dominant genodermatosis and this disease is a geneticall...
Dowling–Degos disease (DDD) and reticulate acropigmentation of Kitamura (RAK) are rare genodermatose...
Dowling-Degos disease (DDD) is an unusual pigmentary disorder usually caused by mutations in keratin...
Dyschromatosis universalis hereditaria (DUH) is a rare pigmentary disorder characterized by the pres...
Herein we report a rare case of classical Dowling-Degos disease (DDD) in a Taiwanese woman. A 23-yea...
A doença de Dowling-Degos é uma genodermatose rara que consiste numa desordem pigmentar reticulada. ...
Reticulate acral and flexural pigmentary disorders are a rare group of pigmentary genodermatoses. We...
Galli-Galli disease is a rare acantholytic variant of Dowling-Degos disease, with few cases reported...
6N/AreservedmixedPiccolo V, Corneli P, Russo T, Danielsson M, Zalaudek I, Argenziano G.Piccolo, V; C...
are rare genodermatosis inherited as an auto-somal dominant trait with variable pene-trance. They ar...
AbstractDyschromatosis universalis hereditaria (DUH) is a rare disease that is inherited both in aut...
Galli-Galli disease is a rare acantholytic variant of Dowling-Degos disease, with few cases reported...