Atypical presentation of familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a patient with a new claudin-16 gene mutation.

Autor: Vianna JGP; Internal Medicine at Cassiano Antonio Moraes Hospital, Federal University of Espírito Santo., Simor TG; Federal University of Espírito Santo., Senna P; Federal University of Espírito Santo., De Bortoli MR; Federal University of Espírito Santo., Costalonga EF; Department of Internal Medicine, Division of Endocrinology, Federal University of Espírito Santo, Vitória, ES., Seguro AC; Department of Nephrology, School of Medicine, University of São Paulo, São Paulo, and., Luchi WM; Department of Internal Medicine, Division of Nephrology, Federal University of Espírito Santo, Vitória, ES, Brazil.

Publikováno v: Clinical nephrology. Case studies [Clin Nephrol Case Stud] 2019 May 16; Vol. 7, pp. 27-34. Date of Electronic Publication: 2019 May 16 (Print Publication: 2019).