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International Journal of Pediatrics
Volume 2012 (2012), Article ID 857136, 5 pages
http://dx.doi.org/10.1155/2012/857136
Review Article

Antenatal Bartter Syndrome: A Review

1Department of Paediatrics, Kasturba Medical College, Manipal University, Udupi District, Manipal 576104, India
2Department of Obstetrics and Gynecology, Kasturba Medical College, Manipal University, Udupi District, Manipal 576104, India

Received 29 July 2011; Revised 8 December 2011; Accepted 21 December 2011

Academic Editor: Raymond Quigley

Copyright © 2012 Y. Ramesh Bhat et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. F. C. Bartter, P. Pronove, J. R. Gill Jr., and R. C. MacCardle, “Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome,” American Journal of Medicine, vol. 33, pp. 811–828, 1962. View at Google Scholar
  2. K. M. Dell and E. D. Avner, “Bartter-Gitelman syndromes and other inherited tubular transport abnormalities,” in Nelson Textbook of Pediatrics, R. M. Kleigman, R. E. Behrman, H. B. Jenson, and B. F. Stanton, Eds., pp. 2201–2202, Saunders, Philadelphia, Pa, USA, 18th edition, 2007. View at Google Scholar
  3. W. Proesmans, “Bartter syndrome and its neonatal variant,” European Journal of Pediatrics, vol. 156, no. 9, pp. 669–679, 1997. View at Publisher · View at Google Scholar · View at Scopus
  4. Y. R. Bhat, G. Vinayaka, R. Vani, K. A. Prashanth, and K. Sreelakshmi, “Antenatal Bartter syndrome: a rare cause of unexplained severe polyhydramnios,” Annals of Tropical Paediatrics, vol. 31, pp. 153–157, 2011. View at Google Scholar
  5. K. Brochard, O. Boyer, A. Blanchard et al., “Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome,” Nephrology Dialysis Transplantation, vol. 24, no. 5, pp. 1455–1464, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  6. H. W. Seyberth and K. P. Schlingmann, “Bartter and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects,” Pediatric Nephrology, vol. 26, pp. 1789–1802, 2011. View at Google Scholar
  7. P.R. Rodrıguez and T. Hasaart, “Hydramnios and observations in Bartter’s syndrome,” Acta Obstetricia et Gynecologica Scandinavica, vol. 61, pp. 477–478, 1982. View at Google Scholar
  8. G. Massa, W. Proesmans, H. Devlieger, K. Vandenberghe, A. van Assche, and E. Eggermont, “Electrolyte composition of the amniotic fluid in Bartter syndrome,” European Journal of Obstetrics & Gynecology and Reproductive Biology, vol. 24, pp. 335–340, 1987. View at Google Scholar
  9. B. Dane, M. Yayla, C. Dane, and A. Cetin, “Prenatal diagnosis of Bartter syndrome with biochemical examination of amniotic fluid: case report,” Fetal Diagnosis and Therapy, vol. 22, no. 3, pp. 206–208, 2007. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  10. J. Rodríguez-Soriano, “Bartter and related syndromes: the puzzle is almost solved,” Pediatric Nephrology, vol. 12, no. 4, pp. 315–327, 1998. View at Publisher · View at Google Scholar · View at Scopus
  11. A. Ohlsson, U. Sieck, W. Cumming, M. Akhtar, and F. Serenius, “A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis,” Acta Paediatrica Scandinavica, vol. 73, no. 6, pp. 868–874, 1984. View at Google Scholar · View at Scopus
  12. W. Proesmans, H. Devlieger, and A. Van Assche, “Bartter syndrome in two siblings - Antenatal and neonatal observations,” International Journal of Pediatric Nephrology, vol. 6, no. 1, pp. 63–70, 1985. View at Google Scholar · View at Scopus
  13. M. J. Dunn, “Prostaglandins and Bartter's syndrome,” Kidney International, vol. 19, no. 1, pp. 86–102, 1981. View at Google Scholar · View at Scopus
  14. M. H. Winterborn, G. J. Hewitt, and M. D. Mitchell, “The role of prostaglandins in Bartter's syndrome,” International Journal of Pediatric Nephrology, vol. 5, no. 1, pp. 31–38, 1984. View at Google Scholar · View at Scopus
  15. D. Landau, H. Shalev, M. Ohaly, and R. Carmi, “Infantile variant of Bartter syndrome and sensorineural deafness: a new autosomal recessive disorder,” American Journal of Medical Genetics, vol. 59, no. 4, pp. 454–459, 1995. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  16. G. Madrigal, P. Saborio, F. Mora, G. Rincon, and L. M. Guay-Woodford, “Bartter syndrome in Costa Rica: a description of 20 cases,” Pediatric Nephrology, vol. 11, no. 3, pp. 296–301, 1997. View at Publisher · View at Google Scholar · View at Scopus
  17. Y. Matsushita, Y. Suzuki, N. Oya et al., “Biochemical examination of mother's urine is useful for prenatal diagnosis of Bartter syndrome,” Prenatal Diagnosis, vol. 19, no. 7, pp. 671–673, 1999. View at Publisher · View at Google Scholar · View at Scopus
  18. J. Rodriguez-Soriano, “Tubular disorders of electrolyte regulation,” in Pediatric Nephrology, E. Avner, W. Harmon, and P. Niaudet, Eds., pp. 729–756, Lippincott Williams and Wilkins, Philadelphia, Pa, USA, 5th edition, 2004. View at Google Scholar
  19. J. Rodriguez-Soriano, “Bartter's syndrome comes of age,” Pediatrics, vol. 103, no. 3, pp. 663–664, 1999. View at Publisher · View at Google Scholar
  20. B. Dane, C. Dane, F. Aksoy, A. Cetin, and M. Yayla, “Antenatal bartter syndrome: analysis of two cases with placental findings,” Fetal and Pediatric Pathology, vol. 29, no. 3, pp. 121–126, 2010. View at Publisher · View at Google Scholar · View at PubMed
  21. M. E. Norton, J. Merrill, B. A. B. Cooper, J. A. Kuller, and R. I. Clyman, “Neonatal complications after the administration of indomethacin for preterm labor,” New England Journal of Medicine, vol. 329, no. 22, pp. 1602–1607, 1993. View at Publisher · View at Google Scholar · View at PubMed
  22. M. Konrad, A. Leonhardt, P. Hensen, W. H. Seyberth, and A. Kockerling, “Prenatal and postnatal management of Hyperprostaglandin E syndrome after genetic diagnosis from amniocytes,” Pediatrics, vol. 103, pp. 678–683, 1999. View at Google Scholar
  23. I. Amirlak and K. P. Dawson, “Bartter syndrome: an overview,” QJM, vol. 93, no. 4, pp. 207–215, 2000. View at Google Scholar
  24. E. Ataoglu, M. Civilibal, A. A. Ozkul, I. G. Varal, E. R. Oktay, and E. Murat, “Indomethacin-induced colon perforation in Bartter's syndrome,” Indian Journal of Pediatrics, vol. 76, no. 3, pp. 322–323, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  25. K. Brochard, O. Boyer, A. Blanchard et al., “Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome,” Nephrology Dialysis Transplantation, vol. 24, no. 5, pp. 1455–1464, 2009. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  26. E. Puricelli, A. Bettinelli, N. Borsa et al., “Long-term follow-up of patients with Bartter syndrome type i and II,” Nephrology Dialysis Transplantation, vol. 25, no. 9, pp. 2976–2981, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  27. S. Reinalter, H. Devlieger, and W. Proesmans, “Neonatal Bartter syndrome: spontaneous resolution of all signs and symptoms,” Pediatric Nephrology, vol. 12, no. 3, pp. 186–188, 1998. View at Publisher · View at Google Scholar · View at Scopus