Bartter Syndrome Masquerading as Acute Kidney Injury in a Neonate

Author:

Jaladi Ravi Teja,Biswas Arnab,Mitra Sonali

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference6 articles.

1. Sinha A, Bagga A. Tubular disorders. In: Srivastava RN, Bagg A, editors. Pediatric Nephrology, 6th edition. Jaypee publishers; 2016. p. 312–16.

2. Dixon BP, Bartter syndrome, inherited tubular transport abnormalities. In: Kliegman, St Geme, Blum, Shah, Tasker, Wilson, editors. Nelsons Textbook of Paediatrics, 21st edition. Elsiever; 2019. p. 2767–9.

3. Kurtz I. Molecular pathogenesis of Bartter’s and Gitelman’s syndromes. Kidney Int. 1998;54:1396–410.

4. Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, et al. Genetic heterogeneity of Bartter’s syndrome revealed by mutations in the K+ channel, ROMK: Classic diseases revisited. Nat Genet. 1996;14:152–6.

5. Laghmani K, Beck BB, Yang SS, Seaayfan E, Wenzel A, Reusch B, et al. Polyhydramnios, transient antenatal Bartter’s syndrome, and MAGED2 mutations. N Engl J Med. 2016;374:1853–63.

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