1.
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