Department of Prosthetic Dentistry, Specialist Clinic Kaniken, Public Dental Health Service, Uppsala, Sweden.
Department of Immunology, Genetics and Pathology, Uppsala University and Uppsala University Hospital, Uppsala, Sweden.
Ups J Med Sci. 2024 Sep 13;129. doi: 10.48101/ujms.v129.10228. eCollection 2024.
The heterogeneous features of enamel renal syndrome (ERS) make diagnosis and treatment challenging. The main symptoms are disturbed amelogenesis and nephrocalcinosis. Bi-allelic likely pathogenic (LP) or pathogenic (P) variants in have been associated with the syndrome since 2012. Affected patients often receive extensive dental treatment because of deviant orofacial morphology. However, knowledge about long-term prognosis and treatment guidelines are still lacking. The complex nature of ERS might endanger both dental and general health. The purpose of this article is to highlight the risks of overlooking the symptoms of the syndrome, and to discuss management strategies, surveillance and prognosis.
We report the management of a case with suspected ERS after initial dental treatment elsewhere with no adjustment for the syndrome. Dental treatment was revised and followed for 8 years. Complementary medical examinations were conducted, and ERS was genetically confirmed, revealing homozygosity for a LP c.755_757del, p.(Phe252del) variant in . The nephrological investigation revealed medullary calcium deposits, normal renal function and hypophosphatemia. Urine analysis revealed hypocitraturia and hypocalciuria. Accordingly, the patient now medicates with potassium citrate to decrease the risk of progressive renal stone formation.
We herein describe a patient with confirmed ERS with an 8-year follow-up. Diagnostic delay until adulthood led to complicated dental treatment. The results of nephrological investigations are presented. The importance of dental and medical multidisciplinary management in syndromic disorders affecting the formation of the enamel is also exemplified. The dental prognosis after rehabilitation is likely affected by anatomical variations and patient cooperation. The prognosis for renal function seems to be good. However, lifelong surveillance of renal function is recommended.
The ethics committee in Uppsala, Sweden, determined that ethical approval was not necessary in this case (2019-04835). Informed consent was obtained from the participant in writing and is documented in the medical records.
釉质肾综合征(ERS)的异质性特征使其诊断和治疗具有挑战性。主要症状是牙釉质形成障碍和肾钙质沉着症。自 2012 年以来,已发现与该综合征相关的 中双等位基因可能致病(LP)或致病(P)变体。由于异常的面型,受影响的患者通常需要接受广泛的牙科治疗。然而,关于长期预后和治疗指南的知识仍然缺乏。ERS 的复杂性可能危及牙齿和整体健康。本文的目的是强调忽视该综合征症状的风险,并讨论管理策略、监测和预后。
我们报告了一例在其他地方进行初始牙科治疗后疑似 ERS 的病例,该病例未对该综合征进行调整。对牙科治疗进行了修正,并随访了 8 年。进行了补充的医学检查,并通过基因检测证实存在 ERS,携带 中的 LP c.755_757del,p.(Phe252del) 变体的纯合性。肾脏检查显示髓质钙沉积、肾功能正常和低磷血症。尿液分析显示低柠檬酸尿症和低钙尿症。因此,目前患者服用枸橼酸钾以降低进行性肾结石形成的风险。
我们在此描述了一例经 8 年随访确诊的 ERS 患者。直到成年才出现诊断延迟,导致复杂的牙科治疗。还介绍了肾脏检查的结果。此外,还举例说明了多学科管理对影响牙釉质形成的综合征性疾病的重要性。修复后的牙齿预后可能受解剖变异和患者合作的影响。肾功能的预后似乎良好,但建议终身监测肾功能。
瑞典乌普萨拉的伦理委员会确定在这种情况下不需要伦理批准(2019-04835)。患者以书面形式获得知情同意,并记录在病历中。