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Familial pityriasis rubra pilaris
rareA 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.
- Identifiers
- MONDO:0008251 OMIM:173200Orphanet:2897
- Causal genes
- CARD14
- Also known as
- Devergie's disease · hereditary pityriasis rubra pilaris · pityriasis rubra pilaris--familial type · PRP
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