Clinical and genetic analysis of Dent disease with nephrotic range albuminuria in Shaanxi, China-Reference-Cited by-同舟云学术

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Clinical and genetic analysis of Dent disease with nephrotic range albuminuria in Shaanxi, China

Published:2019-11-05 Issue:12 Volume:62 Page:1590-1593
ISSN:1674-7305
Container-title:Science China Life Sciences
language:en
Short-container-title:Sci. China Life Sci.

Author:

Bao Ying,Suo Lei,Qian Pei,Huang Huimei,Yang Ying,Tang Jun,Zhang Min,Li Zhijuan,Wang Ying,Liang Nan,Wang Yili

Publisher

Springer Science and Business Media LLC

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Biochemistry, Genetics and Molecular Biology

Link

http://link.springer.com/content/pdf/10.1007/s11427-018-9829-0.pdf

Reference7 articles.

1. Addis, M., Meloni, C., Tosetto, E., Ceol, M., Cristofaro, R., Melis, M.A., Vercelloni, P., Del Prete, D., Marra, G., and Anglani, F. (2013). An atypical Dent’s disease phenotype caused by co-inheritance of mutations at CLCN5 and OCRL genes. Eur J Hum Genet 21, 687–690.

2. Dent, C.E., and Friedman, M. (1964). Hypercalcuric rickets associated with renal tubular damage. Arch Dis Childhood 39, 240–249.

3. Sekine, T., Komoda, F., Miura, K., Takita, J., Shimadzu, M., Matsuyama, T., Ashida, A., and Igarashi, T. (2014). Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA: genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria. Nephrol Dialysis Transplant 29, 376–384.

4. Tosetto, E., Ghiggeri, G.M., Emma, F., Barbano, G., Carrea, A., Vezzoli, G., Torregrossa, R., Cara, M., Ripanti, G., Ammenti, A., et al. (2006). Phenotypic and genetic heterogeneity in Dent’s disease—the results of an Italian collaborative study. Nephrol Dialysis Transplant 21, 2452–2463.

5. van Berkel, Y., Ludwig, M., van Wijk, J.A.E., and Bökenkamp, A. (2017). Proteinuria in Dent disease: a review of the literature. Pediatr Nephrol 32, 1851–1859.

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