Congenital nephrogenic diabetes insipidus due to the mutation in AVPR2 (c.541C>T) in a neonate: A case report

doi:10.12998/wjcc.v8.i24.6418

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Dec 26, 2020 (publication date) through Nov 4, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Dec 26, 2020; 8(24): 6418-6424
Published online Dec 26, 2020. doi: 10.12998/wjcc.v8.i24.6418

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Figure 3 Genetic tests confirmed that the patient’s mother carried the AVPR2 gene mutation c. 541C>T.

Citation: Lin FT, Li J, Xu BL, Yang XX, Wang F. Congenital nephrogenic diabetes insipidus due to the mutation in AVPR2 (c.541C>T) in a neonate: A case report. World J Clin Cases 2020; 8(24): 6418-6424
URL: https://www.wjgnet.com/2307-8960/full/v8/i24/6418.htm
DOI: https://dx.doi.org/10.12998/wjcc.v8.i24.6418