Development of metabolic syndrome at a young age as a manifestation of familial partial lipodystrophy type 3 (PPARG mutation): the first description of its clinical case in Russia

Development of metabolic syndrome at a young age as a manifestation of familial partial lipodystrophy type 3 (PPARG mutation): the first description of its clinical case in Russia

Metabolic syndrome (MS) is extremely common (20%–25% of the world’s population), and its diagnostic criteria are defined and well known. It has been shown that patients who have MS are twice as likely to die from a cardiovascular complication and three times as likely to suffer from it compared with...

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Main Authors: Ekaterina Leonidovna Sorkina, Marina Fedorovna Kalashnikova, Natalya Vyacheslavovna Likhodey, Ekaterina Olegova Koksharova, Dmitry Vladimirovich Ustyuzhanin, Alexander Yuryevich Mayorov, Marina Vladimirovna Shestakova, Anatoly Nikolaevich Tiulpakov
Format: article
Language:EN
RU
Published: Endocrinology Research Centre 2015
Subjects:
metabolic syndrome
familial partial lipodystrophy type 3
pparg
insulin resistance
impaired glucose tolerance
acanthosis nigricans
polycystic ovary syndrome
Nutritional diseases. Deficiency diseases
RC620-627
Online Access:https://doaj.org/article/4fbbd980baef4951b83935980887ef05
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https://doaj.org/article/4fbbd980baef4951b83935980887ef05

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