Atypical familial Papillon-Lefevre syndrome
| dc.contributor.author | Inalöz, HS | |
| dc.contributor.author | Harman, M | |
| dc.contributor.author | Akdeniz, S | |
| dc.contributor.author | Inalöz, SS | |
| dc.contributor.author | Isik, AG | |
| dc.date.accessioned | 2024-04-24T16:24:06Z | |
| dc.date.available | 2024-04-24T16:24:06Z | |
| dc.date.issued | 2001 | |
| dc.department | Dicle Üniversitesi | en_US |
| dc.description.abstract | The Papillon-Lefevre syndrome is a rare autosomal recessive disorder. Consanguinity seems a notable prerequisite. Papillon-Lefevre syndrome manifests in the first 6 months of life with rapidly progressive periodontitis and severe alveolar bone destruction leading to early loss of both the deciduous and permanent teeth in association with palmo-plantar hyperkeratosis. We present two unusual cases of familial Papillon-Lefevre syndrome, one of whom has only late onset of mild skin lesions and the other has severe skin lesions and relatively mild periodontal disease. A number of other cases recently described have also had atypical features. | en_US |
| dc.identifier.doi | 10.1046/j.1468-3083.2001.00121.x | |
| dc.identifier.endpage | 50 | en_US |
| dc.identifier.issn | 0926-9959 | |
| dc.identifier.issue | 1 | en_US |
| dc.identifier.pmid | 11451323 | |
| dc.identifier.scopus | 2-s2.0-0034848523 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 48 | en_US |
| dc.identifier.uri | https://doi.org/10.1046/j.1468-3083.2001.00121.x | |
| dc.identifier.uri | https://hdl.handle.net/11468/16496 | |
| dc.identifier.volume | 15 | en_US |
| dc.identifier.wos | WOS:000169560000017 | |
| dc.identifier.wosquality | Q3 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | en_US |
| dc.publisher | European Acad Dermatology & Venereology | en_US |
| dc.relation.ispartof | Journal of The European Academy of Dermatology and Venereology | |
| dc.relation.publicationcategory | Diğer | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Hyperkeratosis | en_US |
| dc.subject | Papillon-Lefevre Syndrome | en_US |
| dc.subject | Periodontitis | en_US |
| dc.subject | Psoriasiform Lesions | en_US |
| dc.subject | Retinoids | en_US |
| dc.title | Atypical familial Papillon-Lefevre syndrome | en_US |
| dc.title | Atypical familial Papillon-Lefevre syndrome | |
| dc.type | Editorial | en_US |
