Dyschromatosis universalis hereditaria
ORPHA:241· ICD-10 L81.8
Definition
A rare, genetic, pigmentation anomaly of the skin characterized by generalized, irregularly shaped, asymptomatic, hyper- and hypopigmented macules distributed in a reticular pattern involving the trunk, limbs, and sometimes the face. The palms, soles and mucosa are usually not affected. Systemic abnormalities have been rarely reported.
- Inheritance
- Autosomal dominant, Autosomal recessive
- Age of onset
- Childhood, Infancy