MODY3 in the child with type 2 diabetes mellitus phenotype: case report

MODY is a heterogeneous group of diseases that stem from certain genetic mutations and are characterized by beta-cell dysfunction, early clinical onset (before the age of 25) and autosomal dominant inheritance. Nowadays many studies address atypical variants of diabetes mellitus (DM) and consequenti...

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Autores principales: Tamara Leonidovna Kuraeva, Elena Alexandrovich Sechko, Irina Alexandrovna Eremina, O N Ivanova, Sergey Alexandrovich Prokof’ev
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RU
Publicado: Endocrinology Research Centre 2013
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Acceso en línea:https://doaj.org/article/40c9a705f37d46db9d836143ce0af16b
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spelling oai:doaj.org-article:40c9a705f37d46db9d836143ce0af16b2021-11-14T09:00:18ZMODY3 in the child with type 2 diabetes mellitus phenotype: case report2072-03512072-037810.14341/2072-0351-3762https://doaj.org/article/40c9a705f37d46db9d836143ce0af16b2013-06-01T00:00:00Zhttps://www.dia-endojournals.ru/jour/article/view/3762https://doaj.org/toc/2072-0351https://doaj.org/toc/2072-0378MODY is a heterogeneous group of diseases that stem from certain genetic mutations and are characterized by beta-cell dysfunction, early clinical onset (before the age of 25) and autosomal dominant inheritance. Nowadays many studies address atypical variants of diabetes mellitus (DM) and consequential problems in differential diagnosis. Though generally patients with MODY have normal body weight, the ongoing spread of obesity will probably produce comorbid forms and thus alter clinical picture. We present a case of DM in a 13-year-old patient that characterizes development of MODY3 in type 2 DM-like phenotype.Tamara Leonidovna KuraevaElena Alexandrovich SechkoIrina Alexandrovna EreminaO N IvanovaSergey Alexandrovich Prokof’evEndocrinology Research Centrearticlemody3hnf1alphaobesitytype 2 diabetes mellitussulfonylureaNutritional diseases. Deficiency diseasesRC620-627ENRUСахарный диабет, Vol 16, Iss 2, Pp 88-93 (2013)
institution DOAJ
collection DOAJ
language EN
RU
topic mody3
hnf1alpha
obesity
type 2 diabetes mellitus
sulfonylurea
Nutritional diseases. Deficiency diseases
RC620-627
spellingShingle mody3
hnf1alpha
obesity
type 2 diabetes mellitus
sulfonylurea
Nutritional diseases. Deficiency diseases
RC620-627
Tamara Leonidovna Kuraeva
Elena Alexandrovich Sechko
Irina Alexandrovna Eremina
O N Ivanova
Sergey Alexandrovich Prokof’ev
MODY3 in the child with type 2 diabetes mellitus phenotype: case report
description MODY is a heterogeneous group of diseases that stem from certain genetic mutations and are characterized by beta-cell dysfunction, early clinical onset (before the age of 25) and autosomal dominant inheritance. Nowadays many studies address atypical variants of diabetes mellitus (DM) and consequential problems in differential diagnosis. Though generally patients with MODY have normal body weight, the ongoing spread of obesity will probably produce comorbid forms and thus alter clinical picture. We present a case of DM in a 13-year-old patient that characterizes development of MODY3 in type 2 DM-like phenotype.
format article
author Tamara Leonidovna Kuraeva
Elena Alexandrovich Sechko
Irina Alexandrovna Eremina
O N Ivanova
Sergey Alexandrovich Prokof’ev
author_facet Tamara Leonidovna Kuraeva
Elena Alexandrovich Sechko
Irina Alexandrovna Eremina
O N Ivanova
Sergey Alexandrovich Prokof’ev
author_sort Tamara Leonidovna Kuraeva
title MODY3 in the child with type 2 diabetes mellitus phenotype: case report
title_short MODY3 in the child with type 2 diabetes mellitus phenotype: case report
title_full MODY3 in the child with type 2 diabetes mellitus phenotype: case report
title_fullStr MODY3 in the child with type 2 diabetes mellitus phenotype: case report
title_full_unstemmed MODY3 in the child with type 2 diabetes mellitus phenotype: case report
title_sort mody3 in the child with type 2 diabetes mellitus phenotype: case report
publisher Endocrinology Research Centre
publishDate 2013
url https://doaj.org/article/40c9a705f37d46db9d836143ce0af16b
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AT elenaalexandrovichsechko mody3inthechildwithtype2diabetesmellitusphenotypecasereport
AT irinaalexandrovnaeremina mody3inthechildwithtype2diabetesmellitusphenotypecasereport
AT onivanova mody3inthechildwithtype2diabetesmellitusphenotypecasereport
AT sergeyalexandrovichprokofev mody3inthechildwithtype2diabetesmellitusphenotypecasereport
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