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

被引:0
|
作者
Mao, Youying [1 ,2 ]
Zhang, Chenxing [1 ]
Zhou, Zhengyu [1 ]
Zhou, Wei [1 ]
Yin, Lei [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Childrens Med Ctr, Dept Nephrol, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Songjiang Hosp, Dept Pediat, Sch Med, Shanghai, Peoples R China
关键词
Dent disease; CLCN5; end-stage renal disease; rickets; case report; arthralgia; MOLECULAR-WEIGHT PROTEINURIA; MUTATIONS; CHILDREN; CLCN5; NEPHROCALCINOSIS; PHENOTYPE;
D O I
10.1177/03000605241280048
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
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页数:7
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