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Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature

Isolated ACTH deficiency causes life-threatening severe hypoglycemia. A 7-year-old girl with hypoglycemia due to this rare disorder is described. Our patient had undetectable plasma ACTH repeatedly and cortisol 0 mcg/dl before and after ACTH 1-24 stimulation. There was no evidence of other pituitary...

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Autores principales: Torchinsky, Michael Y., Wineman, Robert, Moll, George W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133471/
https://www.ncbi.nlm.nih.gov/pubmed/21760815
http://dx.doi.org/10.1155/2011/784867
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author Torchinsky, Michael Y.
Wineman, Robert
Moll, George W.
author_facet Torchinsky, Michael Y.
Wineman, Robert
Moll, George W.
author_sort Torchinsky, Michael Y.
collection PubMed
description Isolated ACTH deficiency causes life-threatening severe hypoglycemia. A 7-year-old girl with hypoglycemia due to this rare disorder is described. Our patient had undetectable plasma ACTH repeatedly and cortisol 0 mcg/dl before and after ACTH 1-24 stimulation. There was no evidence of other pituitary hormone deficiency. Glucocorticoid replacement therapy resulted in resolution of all symptoms and normalization of blood glucose. Previously published data on isolated ACTH deficiency in children is summarized. Review of the literature showed that the prevalence of this condition could be underestimated in the neonatal period and in Prader-Willi syndrome. Isolated ACTH deficiency occurs in older children as well as in neonates.
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spelling pubmed-31334712011-07-14 Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature Torchinsky, Michael Y. Wineman, Robert Moll, George W. Int J Pediatr Case Report Isolated ACTH deficiency causes life-threatening severe hypoglycemia. A 7-year-old girl with hypoglycemia due to this rare disorder is described. Our patient had undetectable plasma ACTH repeatedly and cortisol 0 mcg/dl before and after ACTH 1-24 stimulation. There was no evidence of other pituitary hormone deficiency. Glucocorticoid replacement therapy resulted in resolution of all symptoms and normalization of blood glucose. Previously published data on isolated ACTH deficiency in children is summarized. Review of the literature showed that the prevalence of this condition could be underestimated in the neonatal period and in Prader-Willi syndrome. Isolated ACTH deficiency occurs in older children as well as in neonates. Hindawi Publishing Corporation 2011 2011-03-30 /pmc/articles/PMC3133471/ /pubmed/21760815 http://dx.doi.org/10.1155/2011/784867 Text en Copyright © 2011 Michael Y. Torchinsky et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Torchinsky, Michael Y.
Wineman, Robert
Moll, George W.
Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature
title Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature
title_full Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature
title_fullStr Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature
title_full_unstemmed Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature
title_short Severe Hypoglycemia due to Isolated ACTH Deficiency in Children: A New Case Report and Review of the Literature
title_sort severe hypoglycemia due to isolated acth deficiency in children: a new case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133471/
https://www.ncbi.nlm.nih.gov/pubmed/21760815
http://dx.doi.org/10.1155/2011/784867
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