Idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life

A preterm female infant born at 27 weeks of gestation with a birth weight of 990 g developed acute hypotonia, apnea, hypotension and bradycardia mimicking septic shock syndrome at 14h after birth. Laboratory tests indicated a severe hypermagnesemia of 45 mg/dL. The renal function, complete blood cou...

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Detalles Bibliográficos
Autores principales: Hyun, Hye Sun, Choi, Hyun Sin, Kim, Jin Kyu, Ahn, So Yoon, Yoo, Hey Soo, Kim, Eun Sun, Chang, Yun Sil, Park, Won Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195797/
https://www.ncbi.nlm.nih.gov/pubmed/22025925
http://dx.doi.org/10.3345/kjp.2011.54.7.310
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author Hyun, Hye Sun
Choi, Hyun Sin
Kim, Jin Kyu
Ahn, So Yoon
Yoo, Hey Soo
Kim, Eun Sun
Chang, Yun Sil
Park, Won Soon
author_facet Hyun, Hye Sun
Choi, Hyun Sin
Kim, Jin Kyu
Ahn, So Yoon
Yoo, Hey Soo
Kim, Eun Sun
Chang, Yun Sil
Park, Won Soon
author_sort Hyun, Hye Sun
collection PubMed
description A preterm female infant born at 27 weeks of gestation with a birth weight of 990 g developed acute hypotonia, apnea, hypotension and bradycardia mimicking septic shock syndrome at 14h after birth. Laboratory tests indicated a severe hypermagnesemia of 45 mg/dL. The renal function, complete blood count and maternal blood concentrations of magnesium were normal, and the blood cultures were negative. The patient recovered with treatment including exchange transfusion. However, the etiology of the severe hypermagnesemia remains unknown.
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spelling pubmed-31957972011-10-24 Idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life Hyun, Hye Sun Choi, Hyun Sin Kim, Jin Kyu Ahn, So Yoon Yoo, Hey Soo Kim, Eun Sun Chang, Yun Sil Park, Won Soon Korean J Pediatr Case Report A preterm female infant born at 27 weeks of gestation with a birth weight of 990 g developed acute hypotonia, apnea, hypotension and bradycardia mimicking septic shock syndrome at 14h after birth. Laboratory tests indicated a severe hypermagnesemia of 45 mg/dL. The renal function, complete blood count and maternal blood concentrations of magnesium were normal, and the blood cultures were negative. The patient recovered with treatment including exchange transfusion. However, the etiology of the severe hypermagnesemia remains unknown. The Korean Pediatric Society 2011-07 2011-07-31 /pmc/articles/PMC3195797/ /pubmed/22025925 http://dx.doi.org/10.3345/kjp.2011.54.7.310 Text en Copyright © 2011 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Hyun, Hye Sun
Choi, Hyun Sin
Kim, Jin Kyu
Ahn, So Yoon
Yoo, Hey Soo
Kim, Eun Sun
Chang, Yun Sil
Park, Won Soon
Idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life
title Idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life
title_full Idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life
title_fullStr Idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life
title_full_unstemmed Idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life
title_short Idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life
title_sort idiopathic severe hypermagnesemia in an extremely low birth weight infant on the first day of life
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195797/
https://www.ncbi.nlm.nih.gov/pubmed/22025925
http://dx.doi.org/10.3345/kjp.2011.54.7.310
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