Gendronneau M, Kérourédan O, Taque S, Sixou J L, Bonnaure-Mallet M
Université Européenne de Bretagne, Université de Rennes 1 and Centre Hospitalier Universitaire de Rennes, Rennes, France.
Eur Arch Paediatr Dent. 2014 Jun;15(3):217-21. doi: 10.1007/s40368-013-0099-3. Epub 2013 Dec 11.
Schimke immuno-osseous dysplasia (SIOD) is a rare, severe, autosomal recessive disorder that results in spondyloepiphyseal dysplasia, renal dysfunction, immunodeficiency, facial dysmorphism and growth failure. Little is known about oral features associated with SIOD. Some of the dental anomalies encountered are specific to SIOD and have only been reported in individuals with SIOD.
This paper describes the clinical and radiographic dental manifestations of SIOD in two Caucasian brothers. Both lived to be about 10 years old. After a variety of symptoms were reported, a diagnosis of SIOD was finally made when the brothers were, respectively, 5 and 8 years old. At that time, dental anomalies, such as dyschromia, bulbous crowns, short and thin roots, had not been taken into account to establish the diagnosis. However, knowledge of the dental features characteristic of this disease could have helped make the diagnosis. Although both were caries- and periodontal disease-free, special attention was focused on prevention, including dietary counselling, plaque control, oral hygiene instructions and the use of fluoridated toothpaste.
FOLLOW-UP: The two patients were followed every 6 months, for over 2 years (until their death), by both a private dentist and a university hospital dentist, which helped them maintain good oral health. Oral hygiene was assessed at each appointment and fissure sealants were placed by the private practitioner on their first permanent molars.
This report describes dental anomalies specific to SIOD that could facilitate diagnosis. Clinicians and dentists should work in collaboration to diagnose and treat children with SIOD. These patients require regular and specific dental management because of their fragile health and their characteristic dental anomalies. Ideally, preventive visits should be scheduled every 6 months in addition to curative visits as needed.
施姆克免疫性骨发育不良(SIOD)是一种罕见的、严重的常染色体隐性疾病,会导致脊椎骨骺发育不良、肾功能障碍、免疫缺陷、面部畸形和生长发育迟缓。关于与SIOD相关的口腔特征知之甚少。所遇到的一些牙齿异常是SIOD所特有的,仅在SIOD患者中报道过。
本文描述了两名白人兄弟SIOD的临床和影像学牙齿表现。两人都活到了大约10岁。在报告了各种症状后,兄弟俩分别在5岁和8岁时最终被诊断为SIOD。当时,诊断时未考虑牙齿异常,如变色、冠部膨大、牙根短而细。然而,了解这种疾病的牙齿特征本可以有助于做出诊断。尽管两人都没有龋齿和牙周疾病,但特别关注预防措施,包括饮食咨询、菌斑控制、口腔卫生指导和使用含氟牙膏。
两名患者由一名私人牙医和一名大学医院牙医每6个月随访一次,持续了两年多(直到他们去世),这有助于他们保持良好的口腔健康。每次就诊时评估口腔卫生情况,私人执业医生为他们的第一恒磨牙放置窝沟封闭剂。
本报告描述了SIOD特有的牙齿异常,这有助于诊断。临床医生和牙医应合作诊断和治疗SIOD患儿。由于这些患者健康状况脆弱且有特征性的牙齿异常,他们需要定期和特殊的牙科管理。理想情况下,除了根据需要进行治疗性就诊外,预防性就诊应每6个月安排一次。