Page last updated: 2024-10-26

eicosapentaenoic acid ethyl ester and Lipodystrophy

eicosapentaenoic acid ethyl ester has been researched along with Lipodystrophy in 1 studies

Lipodystrophy: A collection of heterogenous conditions resulting from defective LIPID METABOLISM and characterized by ADIPOSE TISSUE atrophy. Often there is redistribution of body fat resulting in peripheral fat wasting and central adiposity. They include generalized, localized, congenital, and acquired lipodystrophy.

Research Excerpts

ExcerptRelevanceReference
"Congenital generalized lipodystrophy type 4 (CGL4) is a rare autosomal recessive condition with high rates of morbidity and mortality."1.72Successful treatment of severe hypertriglyceridemia with icosapent ethyl in a case of congenital generalized lipodystrophy type 4. ( Babalola, F; Bulic, A; Curtis, J; Ng, D, 2022)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's1 (100.00)2.80

Authors

AuthorsStudies
Babalola, F1
Ng, D1
Bulic, A1
Curtis, J1

Other Studies

1 other study available for eicosapentaenoic acid ethyl ester and Lipodystrophy

ArticleYear
Successful treatment of severe hypertriglyceridemia with icosapent ethyl in a case of congenital generalized lipodystrophy type 4.
    Journal of pediatric endocrinology & metabolism : JPEM, 2022, Jul-26, Volume: 35, Issue:7

    Topics: Adolescent; Eicosapentaenoic Acid; Female; Humans; Hypertriglyceridemia; Lipodystrophy; Lipodystroph

2022