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. 2023 Jan;38(1):115-117.
doi: 10.1007/s00467-022-05615-0. Epub 2022 Jun 13.

Unexpected finding in kidney biopsy of a child with nephrotic proteinuria: Answers

Meral Torun Bayram  1 , Gizem Yildiz  2 , Ahmet Okay Cağlayan  3 , Ayfer Ulgenalp  3 , Sadiye Mehtat Unlu  4 , Alper Soylu  2 , Salih Kavukcu  2
Affiliations

Unexpected finding in kidney biopsy of a child with nephrotic proteinuria: Answers

Meral Torun Bayram et al. Pediatr Nephrol. 2023 Jan.
No abstract available

Keywords: CLCN5; Child; Dent’s disease; Hypercalciuria; Nephrocalcinosis; Nephrotic proteinuria.

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References

    1. Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL (2015) Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 17:405–424. https://doi.org/10.1038/gim.2015.30 - DOI
    1. Jin YY, Huang LM, Quan XF, Mao JH (2021) Dent disease: classification, heterogeneity and diagnosis. World J Pediatr 17:52–57. https://doi.org/10.1007/s12519-020-00357-1 - DOI
    1. van Berkel Y, Ludwig M, van Wijk JAE, Bökenkamp A (2017) Proteinuria in Dent disease: a review of the literature. Pediatr Nephrol 32:1851–1859. https://doi.org/10.1007/s00467-016-3499-x - DOI
    1. Li F, Yue Z, Xu T, Chen M, Zhong L, Liu T, Jing X, Deng J, Hu B, Liu Y, Wang H, Lai KN, Sun L, Liu J, Maxwell PH, Wang Y (2016) Dent disease in Chinese children and findings from heterozygous mothers: phenotypic heterogeneity, fetal growth, and 10 novel mutations. J Pediatr 174:204-210.e1. https://doi.org/10.1016/j.jpeds.2016.04.007 - DOI
    1. Claverie-Martín F, Ramos-Trujillo E, García-Nieto V (2011) Dent’s disease: clinical features and molecular basis. Pediatr Nephrol 26:693–704. https://doi.org/10.1007/s00467-010-1657-0 - DOI

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