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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Pediatric Endocrinology
2016
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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. |
format | Online Article Text |
id | pubmed-5290178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Society of Pediatric Endocrinology |
record_format | MEDLINE/PubMed |
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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