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Універсальний спадковий дисхроматоз

ORPHA:241· ICD-10 L81.8· Dyschromatosis universalis hereditaria

Визначення(English summary)

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.

Успадкування
Autosomal dominant, Autosomal recessive
Вік початку
Childhood, Infancy