Pediatric Dent disease presenting with rickets and end-stage renal disease: case report and literature review.

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Youying Mao, Chenxing Zhang, Zhengyu Zhou, Wei Zhou, Lei Yin
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引用次数: 0

Abstract

Dent disease is a rare disease with proximal renal tubular dysfunction, and is characterized by low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, and chronic kidney disease. Renal failure slowly progresses and end-stage renal disease may develop in the late decades of life. We report a case of a 15-year-old boy who was diagnosed with Dent disease 1 with a CLCN5 truncating mutation. The patient presented with arthralgia and rickets at the onset of Dent disease and he was diagnosed with end-stage renal disease at the age of 15 years. His only symptoms were arthralgia and rickets during the disease course. The findings in this case suggest that patients with arthralgia and rickets could have a rare cause such as Dent disease.

小儿牙病伴佝偻病和终末期肾病:病例报告和文献综述。
登特病是一种罕见的近端肾小管功能障碍疾病,以低分子量蛋白尿、高钙尿、肾钙化、肾结石和慢性肾病为特征。肾功能衰竭进展缓慢,晚期肾病可能会出现。我们报告了一例 15 岁男孩的病例,他被诊断患有 Dent 病 1,并伴有 CLCN5 截断突变。患者在 Dent 病发时出现关节痛和佝偻病,15 岁时被诊断为终末期肾病。在病程中,他唯一的症状就是关节痛和佝偻病。本病例的研究结果表明,关节痛和佝偻病患者可能有罕见的病因,如 Dent 病。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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