Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing

Symptoms of mild hypoglycemia are easily overlooked especially when there are no complaints from the patients, but it could be a warning sign of an underlying genetic disease. Genetic testing for the entire family is a key step in neonatal hypoglycemia workup.

Detalles Bibliográficos
Autores principales: Baleanu, Felicia, Taujan, Georgiana, Rosu, Mihaela, Kosmopoulou, Olga, Papadopoulou, Blerta Ioanna, Boros, Emese, Iconaru, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731303/
https://www.ncbi.nlm.nih.gov/pubmed/36514475
http://dx.doi.org/10.1002/ccr3.6636
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author Baleanu, Felicia
Taujan, Georgiana
Rosu, Mihaela
Kosmopoulou, Olga
Papadopoulou, Blerta Ioanna
Boros, Emese
Iconaru, Laura
author_facet Baleanu, Felicia
Taujan, Georgiana
Rosu, Mihaela
Kosmopoulou, Olga
Papadopoulou, Blerta Ioanna
Boros, Emese
Iconaru, Laura
author_sort Baleanu, Felicia
collection PubMed
description Symptoms of mild hypoglycemia are easily overlooked especially when there are no complaints from the patients, but it could be a warning sign of an underlying genetic disease. Genetic testing for the entire family is a key step in neonatal hypoglycemia workup.
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spelling pubmed-97313032022-12-12 Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing Baleanu, Felicia Taujan, Georgiana Rosu, Mihaela Kosmopoulou, Olga Papadopoulou, Blerta Ioanna Boros, Emese Iconaru, Laura Clin Case Rep Case Report Symptoms of mild hypoglycemia are easily overlooked especially when there are no complaints from the patients, but it could be a warning sign of an underlying genetic disease. Genetic testing for the entire family is a key step in neonatal hypoglycemia workup. John Wiley and Sons Inc. 2022-12-08 /pmc/articles/PMC9731303/ /pubmed/36514475 http://dx.doi.org/10.1002/ccr3.6636 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Baleanu, Felicia
Taujan, Georgiana
Rosu, Mihaela
Kosmopoulou, Olga
Papadopoulou, Blerta Ioanna
Boros, Emese
Iconaru, Laura
Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing
title Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing
title_full Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing
title_fullStr Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing
title_full_unstemmed Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing
title_short Congenital hyperinsulinism—A case of mild hypoglycemia in an adult, detected by family testing
title_sort congenital hyperinsulinism—a case of mild hypoglycemia in an adult, detected by family testing
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731303/
https://www.ncbi.nlm.nih.gov/pubmed/36514475
http://dx.doi.org/10.1002/ccr3.6636
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