“Neonatal variant” of Bartter syndrome presenting with acidosis

Author:

Ammenti Anita,Montali Simona

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Reference14 articles.

1. Fanconi A, Schachenmann G, Nüssli R, Prader A (1971) Chronic hypokalaemia with growth retardation, normotensive hyperrenin-hyperaldosteronism (Bartter's syndrome), and hypercalciuria. Helv Paediatr Acta 26: 144–163

2. McCredie DA, Rotenberg E, Williams AL (1974) Hypercalciuria in potassium-losing nephropathy: a variant of Bartter's syndrome. Aust Paediatr J 10: 286–295

3. Robson WL, Arbus GS, Balfe JW (1979) Bartter's syndrome. Differentiation into two clinical groups. Am J Dis Child 133: 636–638

4. Dillon MJ, Shah V, Mitchell MD (1979) Bartter's syndrome: 10 cases in childhood. Q J Med 48: 429–446

5. Marlow N, Chiswick ML (1982) Neonatal Bartter's syndrome, indomethacin and necrotising enterocolitis. Acta Paediatr Scand 71: 1031–1032

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1. Association of Mutations in SLC12A1 Encoding the NKCC2 Cotransporter With Neonatal Primary Hyperparathyroidism;The Journal of Clinical Endocrinology & Metabolism;2016-05-01

2. A Case of Antenatal Bartter Syndrome with Sensorineural Deafness;Journal of Pediatric Endocrinology and Metabolism;2010-01

3. A case of Bartter syndrome type I with atypical presentations;Korean Journal of Pediatrics;2010

4. Hereditary Renal Tubular Disorders;Seminars in Nephrology;2009-07

5. Le syndrome de Bartter chez l’enfant : étude de trois observations;Journal de Pédiatrie et de Puériculture;2009-04

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