Skip to main content
Log in

A rare cause of nephrocalcinosis in an infant: Answers

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

A Correction to this article was published on 25 June 2020

This article has been updated

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.

Institutional subscriptions

Fig. 1

Change history

  • 25 June 2020

    Due to an unfortunate error during the processing of this article, the HTML version of this article contained a mistake.

References

  1. Husby S, Koletzko S, Korponay-Szabó I, Kurppa K, Mearin ML, Ribes-Koninckx C, Shamir R, Troncone R, Auricchio R, Castillejo G, Christensen R, Dolinsek J, Gillett P, Hróbjartsson A, Koltai T, Maki M, Nielsen SM, Popp A, Størdal K, Werkstetter K, Wessels M (2012) European Society for Paediatric Gastroenterology, Hepatology and Nutrition guidelines for the diagnosis of coeliac disease. J Pediatr Gastroenterol Nutr 70:141–156. https://doi.org/10.1097/MPG.0b013e31821a23d0

    Article  Google Scholar 

  2. Hoppe B, Kemper MJ (2010) Diagnostic examination of the child with urolithiasis or nephrocalcinosis. Pediatr Nephrol 25:403–413. https://doi.org/10.1007/s00467-008-1073-x

    Article  PubMed  Google Scholar 

  3. Robijn S, Hoppe B, Vervaet BA, D’Haese PC, Verhulst A (2011) Hyperoxaluria: a gut-kidney axis? Kidney Int 80:1146–1158. https://doi.org/10.1038/ki.2011.287

    Article  CAS  PubMed  Google Scholar 

  4. Cuvelier C, Goffin E, Cosyns JP, Wauthier M, de Strihou CY (2015) Enteric hyperoxaluria: an important cause of end-stage kidney disease. Am J Kidney Dis 40:E3.1–E3.6. https://doi.org/10.1053/ajkd.2002.33934

    Article  Google Scholar 

  5. Oh HJ, Ryu KH, Park BJ, Yoon BH (2018) Osteoporosis and osteoporotic fractures in gastrointestinal disease. J Bone Metab 25:213–217. https://doi.org/10.11005/jbm.2018.25.4.213

    Article  PubMed  PubMed Central  Google Scholar 

  6. Mäki M, Mustalahti K, Kokkonen J, Kulmala P, Haapalahti M, Karttunen T, Ilonen J, Laurila K, Dahlbom I, Hansson T, Höpfl P, Knip M (2003) Prevalence of celiac disease among children in Finland. N Engl J Med 348:2517–2524. https://doi.org/10.1056/NEJMoa021687

    Article  PubMed  Google Scholar 

  7. Ciacci C, Spagnuolo G, Tortora R, Bucci C, Franzese D, Zingone F, Cirillo M (2008) Urinary stone disease in adults with celiac disease: prevalence, incidence and urinary determinants. J Urol 180:974–979. https://doi.org/10.1016/j.juro.2008.05.007

    Article  PubMed  Google Scholar 

  8. Ludvigsson JF, Zingone F, Fored M, Ciacci C, Cirillo M (2012) Moderately increased risk of urinary stone disease in patients with biopsy-verified coeliac disease. Aliment Pharmacol Ther 35:477–484. https://doi.org/10.1111/j.1365-2036.2011.04968.x

    Article  CAS  PubMed  Google Scholar 

  9. Yarnell EL (2012) A child with atypical celiac disease and recurrent urolithiasis. Iran J Kidney Dis 6:146–148

    PubMed  Google Scholar 

  10. Mantan M, Dhulika D, Sethi GR (2012) Unusual presentation of celiac disease presenting with renal complications. Indian J Pediatr 79:530–531. https://doi.org/10.1007/s12098-011-0520-z

    Article  PubMed  Google Scholar 

  11. Saccomani MD, Pizzini C, Piacentini GL, Boner AL, Peroni DG (2012) Analysis of urinary parameters as risk factors for nephrolithiasis in children with celiac disease. J Urol 188:566–570. https://doi.org/10.1016/j.juro.2012.04.019

    Article  PubMed  Google Scholar 

  12. Capolongo G, Abul-Ezz S, Moe OW, Sakhaee K (2012) Subclinical celiac disease and crystal-induced kidney disease following kidney transplant. Am J Kidney Dis 60:662–667. https://doi.org/10.1053/j.ajkd.2012.02.342

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Contributions

Dr. Nieto-Vega and Dr. Martin-Masot provided direct care for the patient, collected and assimilated the information in the case, performed the main background search of relevant literature, conceptualized and drafted the initial manuscript, and assisted with the construction of the manuscript and figures. Dr. Rodríguez-Azor, Dr. Martínez-Rivera, and Dr. Navas-López assisted with the construction of the manuscript and figures and contributed significant intellectual content. Ms. Herrador-López collected data, provided important interpretations of the data, and assisted with the drafting of the initial manuscript. All authors reviewed and revised the manuscript, approved the final manuscript as submitted, and agree to be accountable for all aspects of work.

Corresponding author

Correspondence to Francisco Antonio Nieto-Vega.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethics approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Consent for publication

The authors state that the parents of the reported patient gave written informed consent to publish their case.

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/s00467-020-04608-1.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Nieto-Vega, F.A., Martín-Masot, R., Rodríguez-Azor, B. et al. A rare cause of nephrocalcinosis in an infant: Answers. Pediatr Nephrol 36, 79–81 (2021). https://doi.org/10.1007/s00467-020-04615-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00467-020-04615-2

Keywords

Navigation