Clinical Notes
Acute kidney injury in type 3 Bartter syndrome: Angiotensin-converting enzyme inhibitors as a cause
Ryuhei Nagao,
Corresponding Author
Ryuhei Nagao
Department of Pediatrics, Tokyo Medical University, Shinjuku, Tokyo, Japan
Correspondence: Ryuhei Nagao, MD PhD, Department of Pediatrics, Tokyo Medical University, 6-7-1, Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan. Email:
[email protected]Search for more papers by this author Shinzi Suzuki,
Shinzi Suzuki
Department of Pediatrics, Tokyo Medical University, Shinjuku, Tokyo, Japan
Search for more papers by this author Hisashi Kawashima,
Hisashi Kawashima
Department of Pediatrics, Tokyo Medical University, Shinjuku, Tokyo, Japan
Search for more papers by this author Kandai Nozu,
Kandai Nozu
Department of Pediatrics, Kobe University Graduate School of Medicine, Chuo, Kobe, Japan
Search for more papers by this author Kazumoto Iijima,
Kazumoto Iijima
Department of Pediatrics, Kobe University Graduate School of Medicine, Chuo, Kobe, Japan
Search for more papers by this author
Ryuhei Nagao,
Corresponding Author
Ryuhei Nagao
Department of Pediatrics, Tokyo Medical University, Shinjuku, Tokyo, Japan
Correspondence: Ryuhei Nagao, MD PhD, Department of Pediatrics, Tokyo Medical University, 6-7-1, Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan. Email:
[email protected]Search for more papers by this author Shinzi Suzuki,
Shinzi Suzuki
Department of Pediatrics, Tokyo Medical University, Shinjuku, Tokyo, Japan
Search for more papers by this author Hisashi Kawashima,
Hisashi Kawashima
Department of Pediatrics, Tokyo Medical University, Shinjuku, Tokyo, Japan
Search for more papers by this author Kandai Nozu,
Kandai Nozu
Department of Pediatrics, Kobe University Graduate School of Medicine, Chuo, Kobe, Japan
Search for more papers by this author Kazumoto Iijima,
Kazumoto Iijima
Department of Pediatrics, Kobe University Graduate School of Medicine, Chuo, Kobe, Japan
Search for more papers by this author
First published: 23 December 2016
No abstract is available for this article.
References
- 1Fukuyama S, Hiramatsu M, Akagi M, Ohta T. Novel mutations of the chloride channel Kb (ClC-Kb) gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria. J. Clin. Endocrinol. Metab. 2004; 89: 5847–50.
- 2Nozu K, Fu XJ, Nakanishi K et al. Molecular analysis of patients with type III Bartter syndrome: Picking up large heterozygous deletions with semiquantitative PCR. Pediatr. Res. 2007; 62: 364–9.
- 3Abuelo JG. Normotensive ischemic acute renal failure. N. Engl. J. Med. 2007; 357: 797–805.
