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Aggressive periodontitis associated with Kindler syndrome in a large Kindler syndrome pedigree.

Authors :
Yıldırım, Tuba Talo
Kaya, Filiz Acun
Taşkesen, Mustafa
Dündar, Serkan
Bozoğlan, Alihan
Tekin, Gülücağ Giray
Akdeniz, Sedat
Source :
Turkish Journal of Pediatrics; 2017, Vol. 59 Issue 1, p56-61, 6p, 5 Black and White Photographs, 4 Diagrams
Publication Year :
2017

Abstract

Kindler syndrome (KS) is a rare genetic disorder. The clinical features include aggressive periodontal disease and severe desquamative gingivitis. Five individuals with KS were assessed by oral examination, radiographic analysis and periodontal measurements. All the patients' indexes were recorded prior to periodontal treatment and at the end of the 1<superscript>th</superscript>, 3<superscript>th</superscript>, 6<superscript>th</superscript>, 9<superscript>th</superscript> and 12<superscript>th</superscript> month respectively. All the patients had improvement of periodontal status and enhancement in index scores. The affected individuals were previously screened for FERMT1 mutations. KS patients' periodontal disease activity could be taken under control with regular follow-up. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00414301
Volume :
59
Issue :
1
Database :
Supplemental Index
Journal :
Turkish Journal of Pediatrics
Publication Type :
Academic Journal
Accession number :
126445030
Full Text :
https://doi.org/10.24953/turkjped.2017.01.009