PAPILLON-LEFEVRE SYNDROME: A REPORT OF TWO CASES IN A FAMILY

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YAZDANFAR A.; KAVEH K.

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Paper Information

Journal: Iranian Journal of Dermatology Year:2006 | Volume:9 | Issue:3 (37 SUPPLEMENT) Page(s): 1-4

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Information Journal Paper

Title

PAPILLON-LEFEVRE SYNDROME: A REPORT OF TWO CASES IN A FAMILY

Author(s)

YAZDANFAR A. | KAVEH K. | Issue Writer Certificate

Keywords

KERATINIZATION DISORDERQ3

PALMOPLANTAR KERATODERMASQ3

PERIODONTITISQ3

Abstract

Palmoplantar keratodermas are a heterogenous group of diseases, one of them is Papillon- Lefevre Syndrome (PLS). This rare disease is inherited as autosomal recessive and characterized by focal hyperkeratotic plaques on elbows and knees, severe periodontal disease resulting in premature loss of teeth. We report two brothers with PLS who did not have a history of this disease in their family.

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APA: Copy

YAZDANFAR, A., & KAVEH, K.. (2006). PAPILLON-LEFEVRE SYNDROME: A REPORT OF TWO CASES IN A FAMILY. IRANIAN JOURNAL OF DERMATOLOGY, 9(3 (37 SUPPLEMENT)), 1-4. SID. https://sid.ir/paper/57827/en

Vancouver: Copy

YAZDANFAR A., KAVEH K.. PAPILLON-LEFEVRE SYNDROME: A REPORT OF TWO CASES IN A FAMILY. IRANIAN JOURNAL OF DERMATOLOGY[Internet]. 2006;9(3 (37 SUPPLEMENT)):1-4. Available from: https://sid.ir/paper/57827/en

IEEE: Copy

A. YAZDANFAR, and K. KAVEH, “PAPILLON-LEFEVRE SYNDROME: A REPORT OF TWO CASES IN A FAMILY,” IRANIAN JOURNAL OF DERMATOLOGY, vol. 9, no. 3 (37 SUPPLEMENT), pp. 1–4, 2006, [Online]. Available: https://sid.ir/paper/57827/en

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