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A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism

Three infants aged between 38 days and 43 days all presented with poor weight gain, hyponatremia, hyperkalemia, and were diagnosed as having urinary tract infections, which were accompanied by urinary tract malformations in our cases. Hydration and infection treatments were given. A few days after a...

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Autores principales: Ceylan, Dilara, Bayramoğlu, Elvan, Polat, Emine, Erdeve, Şenay Savaş, Çetinkaya, Semra, Aycan, Zehra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Turkish Pediatric Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114610/
https://www.ncbi.nlm.nih.gov/pubmed/34013235
http://dx.doi.org/10.14744/TurkPediatriArs.2020.38159
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author Ceylan, Dilara
Bayramoğlu, Elvan
Polat, Emine
Erdeve, Şenay Savaş
Çetinkaya, Semra
Aycan, Zehra
author_facet Ceylan, Dilara
Bayramoğlu, Elvan
Polat, Emine
Erdeve, Şenay Savaş
Çetinkaya, Semra
Aycan, Zehra
author_sort Ceylan, Dilara
collection PubMed
description Three infants aged between 38 days and 43 days all presented with poor weight gain, hyponatremia, hyperkalemia, and were diagnosed as having urinary tract infections, which were accompanied by urinary tract malformations in our cases. Hydration and infection treatments were given. A few days after admission, hormonal studies revealed normal cortisol and 17-hydroxy progesterone levels and markedly high aldosterone levels, thus the patients were diagnosed as having transient pseudohypoaldosteronism. After the proper treatment was given, the transient pseudohypoaldosteronism resolved. In conclusion, when an infant with urinary tract infection or malformation has electrolyte abnormalities, pediatricians should consider the diagnosis of transient pseudohypoaldosteronism.
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spelling pubmed-81146102021-05-18 A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism Ceylan, Dilara Bayramoğlu, Elvan Polat, Emine Erdeve, Şenay Savaş Çetinkaya, Semra Aycan, Zehra Turk Arch Pediatr Case Report Three infants aged between 38 days and 43 days all presented with poor weight gain, hyponatremia, hyperkalemia, and were diagnosed as having urinary tract infections, which were accompanied by urinary tract malformations in our cases. Hydration and infection treatments were given. A few days after admission, hormonal studies revealed normal cortisol and 17-hydroxy progesterone levels and markedly high aldosterone levels, thus the patients were diagnosed as having transient pseudohypoaldosteronism. After the proper treatment was given, the transient pseudohypoaldosteronism resolved. In conclusion, when an infant with urinary tract infection or malformation has electrolyte abnormalities, pediatricians should consider the diagnosis of transient pseudohypoaldosteronism. Turkish Pediatric Association 2021-01-01 /pmc/articles/PMC8114610/ /pubmed/34013235 http://dx.doi.org/10.14744/TurkPediatriArs.2020.38159 Text en Copyright © 2021 Turkish Pediatric Association https://creativecommons.org/licenses/by-nc/4.0/Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
spellingShingle Case Report
Ceylan, Dilara
Bayramoğlu, Elvan
Polat, Emine
Erdeve, Şenay Savaş
Çetinkaya, Semra
Aycan, Zehra
A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism
title A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism
title_full A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism
title_fullStr A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism
title_full_unstemmed A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism
title_short A rare cause of salt-wasting in early infancy: Transient pseudohypoaldosteronism
title_sort rare cause of salt-wasting in early infancy: transient pseudohypoaldosteronism
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114610/
https://www.ncbi.nlm.nih.gov/pubmed/34013235
http://dx.doi.org/10.14744/TurkPediatriArs.2020.38159
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