Yıldırım Tuba Talo, Kaya Filiz Acun, Taşkesen Mustafa, Dündar Serkan, Bozoğlan Alihan, Tekin Gülücağ Giray, Akdeniz Sedat
Department of Periodontology, Fırat University Faculty of Dentistry, Elazığ, Turkey.
Department of Periodontology, Faculty of Dentistry, Dicle University, Diyarbakır, Turkey.
Turk J Pediatr. 2017;59(1):56-61. doi: 10.24953/turkjped.2017.01.009.
Talo-Yıldırım T, Acun-Kaya F, Taşkesen M, Dündar S, Bozoğlan A, Tekin GG, Akdeniz S. Aggressive periodontitis associated with Kindler syndrome in a large Kindler syndrome pedigree. Turk J Pediatr 2017; 59: 56-61. 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 1th, 3th , 6th, 9th and 12th 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.
塔洛 - 耶尔德勒姆·T、阿昆 - 卡亚·F、塔斯克森·M、敦达尔·S、博佐格兰·A、特金·G·G、阿克德尼兹·S。在一个大型Kindler综合征家系中与Kindler综合征相关的侵袭性牙周炎。《土耳其儿科学杂志》2017年;59:56 - 61。Kindler综合征(KS)是一种罕见的遗传性疾病。临床特征包括侵袭性牙周病和严重的剥脱性龈炎。通过口腔检查、影像学分析和牙周测量对5例KS患者进行了评估。分别在牙周治疗前以及第1、3、6、9和12个月结束时记录所有患者的指标。所有患者的牙周状况均有改善,指标评分提高。之前对受影响个体进行了FERMT1突变筛查。通过定期随访可以控制KS患者的牙周疾病活动。