Familial pityriasis rubra pilaris: a case report
JPAD-Journal of Pakistan Association of Dermatologists. 2013; 23 (1): 83-86
in English
| IMEMR
| ID: emr-126885
ABSTRACT
Pityriasis rubra pilaris [PRP] is a rare papulosquamous disorder of unknown etiology characterized by reddish orange plaques with pityriasiform scaling with follicular keratoses, palmoplantar keratoderma, and occasionally erythroderma. We hereby report a family with five members affected with the condition in three successive generations
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Index:
IMEMR (Eastern Mediterranean)
Language:
English
Journal:
J. Pak. Assoc. Dermatol.
Year:
2013
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