Fetal urine biochemistry in antenatal Bartter syndrome: a case report

Bartter syndrome is a severe inherited tubulopathy responsible for renal salt wasting, and hence electrolyte disorders and dehydration. Prenatally, it is characterized by severe polyhydramnios caused by fetal polyuria. We studied for the first time fetal urine in a Bartter syndrome case and demonstr...

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Autores principales: Rachid, Myriam L., Dreux, Sophie, Czerkiewicz, Isabelle, Deschênes, Georges, Vargas‐Poussou, Rosa, Mahieu‐Caputo, Dominique, Oury, Jean‐François, Muller, Françoise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018593/
https://www.ncbi.nlm.nih.gov/pubmed/27648267
http://dx.doi.org/10.1002/ccr3.471
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author Rachid, Myriam L.
Dreux, Sophie
Czerkiewicz, Isabelle
Deschênes, Georges
Vargas‐Poussou, Rosa
Mahieu‐Caputo, Dominique
Oury, Jean‐François
Muller, Françoise
author_facet Rachid, Myriam L.
Dreux, Sophie
Czerkiewicz, Isabelle
Deschênes, Georges
Vargas‐Poussou, Rosa
Mahieu‐Caputo, Dominique
Oury, Jean‐François
Muller, Françoise
author_sort Rachid, Myriam L.
collection PubMed
description Bartter syndrome is a severe inherited tubulopathy responsible for renal salt wasting, and hence electrolyte disorders and dehydration. Prenatally, it is characterized by severe polyhydramnios caused by fetal polyuria. We studied for the first time fetal urine in a Bartter syndrome case and demonstrated that the tubulopathy is already present at 24 weeks of gestation.
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spelling pubmed-50185932016-09-19 Fetal urine biochemistry in antenatal Bartter syndrome: a case report Rachid, Myriam L. Dreux, Sophie Czerkiewicz, Isabelle Deschênes, Georges Vargas‐Poussou, Rosa Mahieu‐Caputo, Dominique Oury, Jean‐François Muller, Françoise Clin Case Rep Case Reports Bartter syndrome is a severe inherited tubulopathy responsible for renal salt wasting, and hence electrolyte disorders and dehydration. Prenatally, it is characterized by severe polyhydramnios caused by fetal polyuria. We studied for the first time fetal urine in a Bartter syndrome case and demonstrated that the tubulopathy is already present at 24 weeks of gestation. John Wiley and Sons Inc. 2016-08-08 /pmc/articles/PMC5018593/ /pubmed/27648267 http://dx.doi.org/10.1002/ccr3.471 Text en © 2016 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Rachid, Myriam L.
Dreux, Sophie
Czerkiewicz, Isabelle
Deschênes, Georges
Vargas‐Poussou, Rosa
Mahieu‐Caputo, Dominique
Oury, Jean‐François
Muller, Françoise
Fetal urine biochemistry in antenatal Bartter syndrome: a case report
title Fetal urine biochemistry in antenatal Bartter syndrome: a case report
title_full Fetal urine biochemistry in antenatal Bartter syndrome: a case report
title_fullStr Fetal urine biochemistry in antenatal Bartter syndrome: a case report
title_full_unstemmed Fetal urine biochemistry in antenatal Bartter syndrome: a case report
title_short Fetal urine biochemistry in antenatal Bartter syndrome: a case report
title_sort fetal urine biochemistry in antenatal bartter syndrome: a case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018593/
https://www.ncbi.nlm.nih.gov/pubmed/27648267
http://dx.doi.org/10.1002/ccr3.471
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