Congenital Hyperinsulinism: the Possibilities of Modern Diagnosis and Treatment

Congenital hyperinsulinism (CHI) — one of the main causes underlying the development of persistent hypoglycemic conditions in childhood. The article presents the experience of diagnosis and treatment in patients with CHI. We have examined 7 children diagnosed with СHI aged 1 month to 1.5 years. For...

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Main Author: Ye.V. Hloba
Format: Article
Language:English
Published: Publishing House Zaslavsky 2015-04-01
Series:Mìžnarodnij Endokrinologìčnij Žurnal
Subjects:
Online Access:http://iej.zaslavsky.com.ua/article/view/75290
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spelling doaj-e4fad094c6fc46e0be9bc4319d0b9c272020-11-24T21:21:48ZengPublishing House ZaslavskyMìžnarodnij Endokrinologìčnij Žurnal2224-07212307-14272015-04-01113.6716617010.22141/2224-0721.3.67.2015.7529075290Congenital Hyperinsulinism: the Possibilities of Modern Diagnosis and TreatmentYe.V. Hloba0Ukrainian Scientific and Practical Centre for Endocrine Surgery, Transplantation of Endocrine Organs and Tissues of Ministry of Healthcare of Ukraine, KyivCongenital hyperinsulinism (CHI) — one of the main causes underlying the development of persistent hypoglycemic conditions in childhood. The article presents the experience of diagnosis and treatment in patients with CHI. We have examined 7 children diagnosed with СHI aged 1 month to 1.5 years. For diagnosing CHI, we have used routine clinical and laboratory investigations, as well as molecular genetic and instrumental diagnostics (18F-DOPA positron emission tomography). Molecular genetic testing confirmed the diagnosis of CHI in 6 children. All 7 children with CHI had various resistance to conservative treatment, had a different degree of psychomotor development and seizures. Of them, 6 children underwent surgery with achievement of normoglycemia. Genetic testing and 18F-DOPA positron emission tomography should be carried out in all children with hypoglycemia and increased or normal levels of C-peptide and insulin to clarify the type of CHI. Further development of genetic diagnostics is necessary to find new CHI genes. Surgical treatment may be a treatment of choice in children with CHI, particularly in its focal form.http://iej.zaslavsky.com.ua/article/view/75290congenital hyperinsulinismhypoglycemiachildrendiagnosis and treatment
collection DOAJ
language English
format Article
sources DOAJ
author Ye.V. Hloba
spellingShingle Ye.V. Hloba
Congenital Hyperinsulinism: the Possibilities of Modern Diagnosis and Treatment
Mìžnarodnij Endokrinologìčnij Žurnal
congenital hyperinsulinism
hypoglycemia
children
diagnosis and treatment
author_facet Ye.V. Hloba
author_sort Ye.V. Hloba
title Congenital Hyperinsulinism: the Possibilities of Modern Diagnosis and Treatment
title_short Congenital Hyperinsulinism: the Possibilities of Modern Diagnosis and Treatment
title_full Congenital Hyperinsulinism: the Possibilities of Modern Diagnosis and Treatment
title_fullStr Congenital Hyperinsulinism: the Possibilities of Modern Diagnosis and Treatment
title_full_unstemmed Congenital Hyperinsulinism: the Possibilities of Modern Diagnosis and Treatment
title_sort congenital hyperinsulinism: the possibilities of modern diagnosis and treatment
publisher Publishing House Zaslavsky
series Mìžnarodnij Endokrinologìčnij Žurnal
issn 2224-0721
2307-1427
publishDate 2015-04-01
description Congenital hyperinsulinism (CHI) — one of the main causes underlying the development of persistent hypoglycemic conditions in childhood. The article presents the experience of diagnosis and treatment in patients with CHI. We have examined 7 children diagnosed with СHI aged 1 month to 1.5 years. For diagnosing CHI, we have used routine clinical and laboratory investigations, as well as molecular genetic and instrumental diagnostics (18F-DOPA positron emission tomography). Molecular genetic testing confirmed the diagnosis of CHI in 6 children. All 7 children with CHI had various resistance to conservative treatment, had a different degree of psychomotor development and seizures. Of them, 6 children underwent surgery with achievement of normoglycemia. Genetic testing and 18F-DOPA positron emission tomography should be carried out in all children with hypoglycemia and increased or normal levels of C-peptide and insulin to clarify the type of CHI. Further development of genetic diagnostics is necessary to find new CHI genes. Surgical treatment may be a treatment of choice in children with CHI, particularly in its focal form.
topic congenital hyperinsulinism
hypoglycemia
children
diagnosis and treatment
url http://iej.zaslavsky.com.ua/article/view/75290
work_keys_str_mv AT yevhloba congenitalhyperinsulinismthepossibilitiesofmoderndiagnosisandtreatment
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