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Systemic primary carnitine deficiency with hypoglycemic encephalopathy

Acute hypoglycemia in children is not an uncommon disease that can be encountered in the Emergency Department. Most cases of childhood hypoglycemia are caused by ketotic hypoglycemia due to missed meals. Often, hypoketotic hypoglycemia can also occur, which suggests hyperinsulinemia or a defect in f...

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Autores principales: Jun, Jae Sung, Lee, Eun Joo, Park, Hyung Doo, Kim, Hae Sook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290178/
https://www.ncbi.nlm.nih.gov/pubmed/28164076
http://dx.doi.org/10.6065/apem.2016.21.4.226
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author Jun, Jae Sung
Lee, Eun Joo
Park, Hyung Doo
Kim, Hae Sook
author_facet Jun, Jae Sung
Lee, Eun Joo
Park, Hyung Doo
Kim, Hae Sook
author_sort Jun, Jae Sung
collection PubMed
description Acute hypoglycemia in children is not an uncommon disease that can be encountered in the Emergency Department. Most cases of childhood hypoglycemia are caused by ketotic hypoglycemia due to missed meals. Often, hypoketotic hypoglycemia can also occur, which suggests hyperinsulinemia or a defect in fatty acid oxidation. Carnitine is essential for long chain fatty acids transfer into mitochondria for oxidation. We present a case of systemic primary carnitine deficiency who presented with seizures due to hypoketotic hypoglycemia.
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spelling pubmed-52901782017-02-03 Systemic primary carnitine deficiency with hypoglycemic encephalopathy Jun, Jae Sung Lee, Eun Joo Park, Hyung Doo Kim, Hae Sook Ann Pediatr Endocrinol Metab Case Report Acute hypoglycemia in children is not an uncommon disease that can be encountered in the Emergency Department. Most cases of childhood hypoglycemia are caused by ketotic hypoglycemia due to missed meals. Often, hypoketotic hypoglycemia can also occur, which suggests hyperinsulinemia or a defect in fatty acid oxidation. Carnitine is essential for long chain fatty acids transfer into mitochondria for oxidation. We present a case of systemic primary carnitine deficiency who presented with seizures due to hypoketotic hypoglycemia. The Korean Society of Pediatric Endocrinology 2016-12 2016-12-31 /pmc/articles/PMC5290178/ /pubmed/28164076 http://dx.doi.org/10.6065/apem.2016.21.4.226 Text en © 2016 Annals of Pediatric Endocrinology & Metabolism http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jun, Jae Sung
Lee, Eun Joo
Park, Hyung Doo
Kim, Hae Sook
Systemic primary carnitine deficiency with hypoglycemic encephalopathy
title Systemic primary carnitine deficiency with hypoglycemic encephalopathy
title_full Systemic primary carnitine deficiency with hypoglycemic encephalopathy
title_fullStr Systemic primary carnitine deficiency with hypoglycemic encephalopathy
title_full_unstemmed Systemic primary carnitine deficiency with hypoglycemic encephalopathy
title_short Systemic primary carnitine deficiency with hypoglycemic encephalopathy
title_sort systemic primary carnitine deficiency with hypoglycemic encephalopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290178/
https://www.ncbi.nlm.nih.gov/pubmed/28164076
http://dx.doi.org/10.6065/apem.2016.21.4.226
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