Hypokalemic Salt-Losing Tubulopathy With Chronic Renal Failure and Sensorineural Deafness
Author:
Affiliation:
1. From the Departments of Pediatrics, Philipps-University, Marburg;
2. School of Medicine, Hannover;
3. Hospital Sankt-Jürgen-Strasse, Bremen;
4. Elisabeth-Hospital, Essen;
5. Charité, Berlin; and
6. Albert-Ludwigs-University, Freiburg, Germany.
Abstract
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology and Child Health
Link
https://publications.aap.org/pediatrics/article-pdf/108/1/e5/893491/e5.pdf
Reference41 articles.
1. Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome.;Seyberth;J Pediatr,1985
2. Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes.;Károlyi;Hum Mol Genet,1997
3. Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome.;Vargas-Poussou;Am J Hum Genet,1998
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