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Papillon-Lefevre syndrome: a case report.

Identifieur interne : 001A60 ( PubMed/Checkpoint ); précédent : 001A59; suivant : 001A61

Papillon-Lefevre syndrome: a case report.

Auteurs : P. Subramaniam [Inde] ; S. Mathew ; K K Gupta

Source :

RBID : pubmed:19008627

Descripteurs français

English descriptors

Abstract

Papillon-Lefevre syndrome is a rare autosomal recessive genetic disorder. The clinical manifestations include palmer planter hyperkeratosis with precocious progressive periodontal disease that results in premature exfoliation of primary and permanent dentitions. Patients are often edentulous at an early age. This is a case report of prosthodontic rehabilitation of a 15-year-old girl with Papillon-Lefevre syndrome.

PubMed: 19008627


Affiliations:


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pubmed:19008627

Le document en format XML

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<name sortKey="Subramaniam, P" sort="Subramaniam, P" uniqKey="Subramaniam P" first="P" last="Subramaniam">P. Subramaniam</name>
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<nlm:affiliation>Department of Pedodontics and Preventive Dentistry, The Oxford Dental College, Hospital and Research Centre, Bommanahalli, Hosur Road, Bangalore - 560 068, Karnataka, India. drpriyapedo@yahoo.com</nlm:affiliation>
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<div type="abstract" xml:lang="en">Papillon-Lefevre syndrome is a rare autosomal recessive genetic disorder. The clinical manifestations include palmer planter hyperkeratosis with precocious progressive periodontal disease that results in premature exfoliation of primary and permanent dentitions. Patients are often edentulous at an early age. This is a case report of prosthodontic rehabilitation of a 15-year-old girl with Papillon-Lefevre syndrome.</div>
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