Skip to main content
Log in

Hypokalemia and hearing loss in a 3-year-old boy: Answers

  • Clinical Quiz
  • Published:
Pediatric Nephrology Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Casazza G, Meier JD (2017) Evaluation and management of syndromic congenital hearing loss. Curr Opin Otolaryngol Head Neck Surg 25:378–384. https://doi.org/10.1097/MOO.0000000000000397

    Article  PubMed  Google Scholar 

  2. Grindle CR (2014) Pediatric hearing loss. Pediatr Rev 35:456–463. https://doi.org/10.1542/pir.35-11-456

    Article  PubMed  Google Scholar 

  3. Prosser JD, Cohen AP, Greinwald JH (2015) Diagnostic evaluation of children with sensorineural hearing loss. Otolaryngol Clin N Am 8:975–982. https://doi.org/10.1016/j.otc.2015.07.004

    Article  Google Scholar 

  4. Broomfield SJ, Bruce IA, Henderson L, Ramsden RT, Green KM (2013) Cochlear implantation in children with syndromic deafness. Int J Pediatr Otorhinolaryngol 77:1312–1316. https://doi.org/10.1016/j.ijporl.2013.05.022

    Article  PubMed  Google Scholar 

  5. Bartter FC, Pronove P, Gill JR Jr, Maccardle RC (1962) Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome. Am J Med 33:811–828. https://doi.org/10.1016/0002-9343(62)90214-0

    Article  CAS  PubMed  Google Scholar 

  6. Fulchiero R, Seo-Mayer P (2019) Bartter syndrome and Gitelman syndrome. Pediatr Clin N Am 66:121–134. https://doi.org/10.1016/j.pcl.2018.08.010

    Article  Google Scholar 

  7. Cunha TDS, Heilberg IP (2018) Bartter syndrome: causes, diagnosis, and treatment. Int J Nephrol Renov Dis 11:291–301. https://doi.org/10.2147/IJNRD.S155397

    Article  Google Scholar 

  8. Janssen AG, Scholl U, Domeyer C, Nothmann D, Leinenweber A, Fahlke C (2009) Disease-causing dysfunctions of barttin in Bartter syndrome type IV. J Am Soc Nephrol 20:145–153. https://doi.org/10.1681/ASN.2008010102

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Miyamura N, Matsumoto K, Taguchi T, Tokunaga H, Nishikawa T, Nishida K, Toyonaga T, Sakakida M, Araki E (2003) Atypical Bartter syndrome with sensorineural deafness with G47R mutation of the beta-subunit for ClC-Ka and ClC-Kb chloride channels, barttin. J Clin Endocrinol Metab 88:781–786. https://doi.org/10.1210/jc.2002-021398

    Article  CAS  PubMed  Google Scholar 

  10. García-Nieto V, Flores C, Luis-Yanes MI, Gallego E, Villar J, Claverie-Martín F (2006) Mutation G47R in the BSND gene causes Bartter syndrome with deafness in two Spanish families. Pediatr Nephrol 21:643–648. https://doi.org/10.1007/s00467-006-0062-1

    Article  PubMed  Google Scholar 

  11. Lee HS, Cheong HI, Ki CS (2010) A case of antenatal Bartter syndrome with sensorineural deafness. J Pediatr Endocrinol Metab 23:1077–1081. https://doi.org/10.1515/jpem.2010.170

    Article  CAS  PubMed  Google Scholar 

  12. Zaffanello M, Taranta A, Palma A, Bettinelli A, Marseglia GL, Emma F (2006) Type IV Bartter syndrome: report of two new cases. Pediatr Nephrol 21:766–770. https://doi.org/10.1007/s00467-006-0090-x

    Article  PubMed  Google Scholar 

  13. Ozlu F, Yapicioğlu H, Satar M, Narli N, Ozcan K, Buyukcelik M, Konrad M, Demirhan O (2006) Barttin mutations in antenatal Bartter syndrome with sensorineural deafness. Pediatr Nephrol 21:1056–1057. https://doi.org/10.1007/s00467-006-0108-4

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

OYA and FSC were the major contributors in writing the manuscript. FSC, OYA, GK, SAT, and USB were involved in clinical monitoring of the patient. SC made the genetic analysis. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Fatma Semsa Cayci.

Ethics declarations

Conflict of interest

The authors declare that they have no conflicts of interest.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

This refers to the article that can be found at https://doi.org/10.1007/s00467-019-04379-4.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Aksoy, O.Y., Cayci, F.S., Ceylaner, S. et al. Hypokalemia and hearing loss in a 3-year-old boy: Answers. Pediatr Nephrol 35, 617–618 (2020). https://doi.org/10.1007/s00467-019-04383-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00467-019-04383-8

Navigation