Reticulate pigmentary disorders (RPDs) are a group of inherited and acquired skin
conditions characterized by hyperpigmented and/or hypopigmented macules. Inherited …

Reticulated pigmentation is a unique pigmentary change caused by a heterogeneous group
of hereditary and acquired disorders. This pigmentation is characterized by a mottled …

In this chapter, skin conditions of the breast are described including ones common and
others involving the breast as an uncommon site and difficult for diagnosis. These conditions …

Purpose Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant
inherited pigmentary dermatosis. The gene responsible for DSH has been identified as …

Dyschromatosis universalis hereditaria is a rare inherited pigmentary disorder. It has a
characteristic reticulate pigmentation involving the entire body, with acral sparing. The case …

Dowling-Degos disease (DDD) is an extremely rare hereditary skin condition characterized
by the development of painless, small-sized pigmented patches known as macules or …

Dyschromatosis universalis hereditaria (DUH) is a rare genodermatoses characterized by
hyperpigmented and hypopigmented macules inherited most commonly in autosomal …

Background Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant
inherited pigmentary dermatosis characterized by a mixture of hyperpigmented and …

Dyschromatosis universalis hereditaria (DUH) is a rare genodermatosis where the affected
manifests mottled pigmentation with intermingled hyper-and hypo-pigmented macules. On …

ABSTRACT Dyschromatosis Universalis Hereditaria is a rare genodermatoses
characterised by hyperpigmented and hypopigmented macules which are variable in size …