SUN-LB111 Comparison of Phenotype and Metabolic Abnormalities Among Familial Partial Lipodystrophy Due to LMNA or PPARG Variants

Familial partial lipodystrophy (FPLD), a rare autosomal dominant disorder, is characterized by marked loss of subcutaneous (sc) fat from the extremities, and predisposition to insulin resistance, diabetes mellitus, dyslipidemia and hepatic steatosis. FPLD2 and FPLD3 due to causal variants in LMNA an...

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Bibliografische gegevens
Gepubliceerd in:J Endocr Soc
Hoofdauteurs: Vasandani, Chandna, Li, Xilong, Sekizkardes, Hilal, Brown, Rebecca, Garg, Abhimanyu
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2020
Onderwerpen:
Diabetes Mellitus and Glucose Metabolism
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7208329/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.2312
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