A case of enamel renal syndrome from a novel genetic mutation, multidisciplinary management and long-term prognosis.

IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Upsala journal of medical sciences Pub Date : 2024-09-13 eCollection Date: 2024-01-01 DOI:10.48101/ujms.v129.10228
Maria Erkapers, Carina Frykholm, Hans Furuland, Susanna Segerström, Andreas Thor
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Abstract

Background: 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 FAM20A 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.

Case presentation: 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 FAM20A. 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.

Conclusion: 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.

Registration: 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.

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一例新型基因突变引起的釉肾综合征、多学科治疗和长期预后。
背景:釉肾综合征(ERS)的特征多种多样,给诊断和治疗带来了挑战。其主要症状是成釉障碍和肾钙化。自2012年以来,FAM20A的双等位基因可能致病(LP)或致病(P)变异与该综合征有关。由于口面部形态异常,受影响的患者通常需要接受广泛的牙科治疗。然而,有关长期预后和治疗指南的知识仍然缺乏。ERS 的复杂性可能会危及牙齿和全身健康。本文旨在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:我们报告了一例疑似 ERS 患者的治疗情况,该患者最初在其他地方接受牙科治疗,但未对该综合征进行调整。对牙科治疗进行了调整,并随访了 8 年。我们对该病例进行了补充医学检查,并对 ERS 进行了遗传学确诊,发现该病例的 FAM20A 基因存在 LP c.755_757del、p.(Phe252del) 变异。肾病检查发现髓质钙沉积、肾功能正常和低磷血症。尿液分析表明患者存在低钙尿和低钙尿。因此,患者现在服用枸橼酸钾,以降低肾结石逐渐形成的风险:我们在此描述了一名随访 8 年的确诊 ERS 患者。由于诊断延误,直到成年后才进行复杂的牙科治疗。本文介绍了肾病检查的结果。此外,还举例说明了牙科和医学多学科管理对影响釉质形成的综合症的重要性。牙科康复后的预后可能会受到解剖学变化和患者合作的影响。肾功能的预后似乎良好。不过,建议终生监测肾功能:瑞典乌普萨拉市伦理委员会认为本病例无需获得伦理批准(2019-04835)。知情同意书以书面形式获得,并记录在病历中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Upsala journal of medical sciences
Upsala journal of medical sciences 医学-医学:内科
CiteScore
5.60
自引率
0.00%
发文量
31
审稿时长
6-12 weeks
期刊介绍: Upsala Journal of Medical Sciences is published for the Upsala Medical Society. It has been published since 1865 and is one of the oldest medical journals in Sweden. The journal publishes clinical and experimental original works in the medical field. Although focusing on regional issues, the journal always welcomes contributions from outside Sweden. Specially extended issues are published occasionally, dealing with special topics, congress proceedings and academic dissertations.
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