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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Endocrinology Research Centre
2013
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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) |
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mody3 hnf1alpha obesity type 2 diabetes mellitus sulfonylurea Nutritional diseases. Deficiency diseases RC620-627 |
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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 |
work_keys_str_mv |
AT tamaraleonidovnakuraeva mody3inthechildwithtype2diabetesmellitusphenotypecasereport AT elenaalexandrovichsechko mody3inthechildwithtype2diabetesmellitusphenotypecasereport AT irinaalexandrovnaeremina mody3inthechildwithtype2diabetesmellitusphenotypecasereport AT onivanova mody3inthechildwithtype2diabetesmellitusphenotypecasereport AT sergeyalexandrovichprokofev mody3inthechildwithtype2diabetesmellitusphenotypecasereport |
_version_ |
1718429578325655552 |