Papillon-Lefevre syndrome: case report
JPAD-Journal of Pakistan Association of Dermatologists. 2017; 27 (2): 187-191
in English
| IMEMR
| ID: emr-190408
ABSTRACT
Papillon-Lefevre syndrome [PLS] is a rare genodermatosis of autosomal recessive inheritance manifesting as palmoplantar hyperkeratosis with periodontitis. A 4-year old Iranian girl was referred to the Mazandaran University Hospital, Sari complaining of well-demarcated, psoriasiform, yellowish, keratotic plaques over the skin of her palms and soles with transgrediens. For cutaneous lesions, she was treated with oral acitretin 0.5 mg/kg/day and topical keratolytic 5% salicylic acid in combination with 10% urea
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Index:
IMEMR (Eastern Mediterranean)
Language:
English
Journal:
J. Pak. Assoc. Dermatol.
Year:
2017
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