Familial partial lipodystrophy (Dunnigan syndrome) due to LMNA gene mutation: The first description of its clinical case in Russia

Familial partial lipodystrophy (Dunnigan syndrome) due to LMNA gene mutation: The first description of its clinical case in Russia

Hereditary lipodystrophies (HLD) are a heterogeneous group of rare diseases characterized by a complete or partial loss of subcutaneous fat and by the development of metabolic disturbances: diabetes mellitus with obvious insulin resistance and acanthosis nigricans, dyslipidemia, hepatic steatosis, h...

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Bibliographic Details
Main Authors: E L Sorkina, M F Kalashnikova, G A Melnichenko, A N Tyulpakov
Format: Article
Language:Russian
Published: "Consilium Medicum" Publishing house 2015-03-01
Series:Терапевтический архив
Subjects:
lipodystrophy
lmna
insulin resistance
diabetes mellitus
acanthosis nigricans
Online Access:https://ter-arkhiv.ru/0040-3660/article/view/31730

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