"Papillon-Lefevre Disease" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Rare, autosomal recessive disorder occurring between the first and fifth years of life. It is characterized by palmoplantar keratoderma with periodontitis followed by the premature shedding of both deciduous and permanent teeth. Mutations in the gene for CATHEPSIN C have been associated with this disease.
| Descriptor ID |
D010214
|
| MeSH Number(s) |
C16.320.850.475.600 C17.800.428.435.600 C17.800.827.475.600
|
| Concept/Terms |
Papillon-Lefevre Disease- Papillon-Lefevre Disease
- Papillon Lefevre Disease
- Keratosis Palmoplantaris with Periodontopathia
- Papillon-Lefevre Syndrome
- Papillon Lefevre Syndrome
- Keratosis Palmoplantar Periodontopathy
- Keratosis Palmoplantar Periodontopathies
- Palmoplantar Periodontopathies, Keratosis
|
Below are MeSH descriptors whose meaning is more general than "Papillon-Lefevre Disease".
Below are MeSH descriptors whose meaning is more specific than "Papillon-Lefevre Disease".
This graph shows the total number of publications written about "Papillon-Lefevre Disease" by people in this website by year, and whether "Papillon-Lefevre Disease" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 0 | 1 | 1 |
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Below are the most recent publications written about "Papillon-Lefevre Disease" by people in Profiles.
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Sollecito TP, Sullivan KE, Pinto A, Stewart J, Korostoff J. Systemic conditions associated with periodontitis in childhood and adolescence. A review of diagnostic possibilities. Med Oral Patol Oral Cir Bucal. 2005 Mar-Apr; 10(2):142-50.