Papillon-Lefèvre syndrome: report of six patients and identification of a novel mutation

Author:

Tekin Burak1,Yucelten Deniz1,Beleggia Filippo2,Sarig Ofer3,Sprecher Eli34

Affiliation:

1. Department of Dermatology; Marmara University School of Medicine; Istanbul Turkey

2. Institute of Human Genetics; University of Cologne; Cologne Germany

3. Department of Dermatology; Tel Aviv Sourasky Medical Center; Tel Aviv University; Tel Aviv Israel

4. Department of Human Molecular Genetics & Biochemistry; Sackler Faculty of Medicine; Tel Aviv University; Tel Aviv Israel

Publisher

Wiley

Subject

Dermatology

Reference24 articles.

1. Deux cas de kératodermie palmaire et plantaire symétrique familiale (maladie de Meleda) chez le frère et la soeur. Coexistence dans les deux cas daltérations dentaires graves;Papillon;Bull Soc Fr Dermatol Syph,1924

2. The syndrome of palmar-plantar hyperkeratosis and premature periodontal destruction of the teeth. A clinical and genetic analysis of the Papillon-Lefèvre syndrome;Gorlin;J Pediatr,1964

3. The Papillon-Lefèvre syndrome: keratosis palmoplantaris with periodontopathy. Report of a case and review of the cases in the literature;Haneke;Hum Genet,1979

4. Dermatologic and oral findings in a cohort of 47 patients with Papillon-Lefèvre syndrome;Ullbro;J Am Acad Dermatol,2003

5. Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome;Hart;J Med Genet,1999

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