Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family.

@article{Sandhu2004DowlingDegosDW,
  title={Dowling-Degos disease with dyschromatosis universalis hereditaria-like pigmentation in a family.},
  author={Kamaldeep Sandhu and Abir Saraswat and Amrinderjit J Kanwar},
  journal={Journal of the European Academy of Dermatology and Venereology : JEADV},
  year={2004},
  volume={18 6},
  pages={702-4}
}
Dowling-Degos disease is a rare autosomal dominant inherited pigmentary disorder characterized by reticulate pigmentation of the flexures, prominent comedone like lesions and pitted scars. Dyschromatosis universalis hereditaria is characterized by the presence of hypopigmented as well as hyperpigmented macules. We report a family showing features of both these diseases.