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Up to: DNA repair disease · Hereditary photodermatosis

Xeroderma pigmentosum

Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by extreme sensitivity to ultraviolet (UV)-induced changes in the skin and eyes, and multiple skin cancers. It is subdivided into 8 complementation groups, according to the affected gene: classical XP (XPA to XPG) and XP variant (XPV).

4 trials tagged with this condition →

Xeroderma pigmentosum group F 1 trial
Xeroderma pigmentosum variant type 1 trial
Xeroderma pigmentosum group A 0 trials
Xeroderma pigmentosum group B 0 trials
Xeroderma pigmentosum group C 0 trials
Xeroderma pigmentosum group D 0 trials
Xeroderma pigmentosum group E 0 trials
Xeroderma pigmentosum group G 0 trials
Xeroderma pigmentosum, autosomal dominant, mild 0 trials
Xeroderma pigmentosum, complementation group J 0 trials