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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Dades bibliogràfiques
Publicat a:J Endocr Soc
Autors principals: Vasandani, Chandna, Li, Xilong, Sekizkardes, Hilal, Brown, Rebecca, Garg, Abhimanyu
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2020
Matèries:
Diabetes Mellitus and Glucose Metabolism
Accés en línia: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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