Familial pityriasis rubra pilaris

MONDO:0008251

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.

Also known as: pityriasis rubra pilaris, Devergie's disease, PRP, hereditary pityriasis rubra pilaris, pityriasis rubra pilaris--familial type

15 clinical trials for this condition and its sub-types.

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