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Up to: Hereditary skin disorder · Pityriasis rubra pilaris

Familial pityriasis rubra pilaris

A rare chronic papulosquamous disorder of unknown etiology characterized by small follicular papules, scaly red-orange patches, and palmoplantar hyperkeratosis, which may progress to plaques or erythroderma. Although most of the cases are sporadic and acquired, a familial form of the disease exists.

10 trials tagged with this condition →

This condition has no sub-types.