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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Detalles Bibliográficos
Autores principales: Vasandani, Chandna, Li, Xilong, Sekizkardes, Hilal, Brown, Rebecca, Garg, Abhimanyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Diabetes Mellitus and Glucose Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208329/
http://dx.doi.org/10.1210/jendso/bvaa046.2312

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7208329/
http://dx.doi.org/10.1210/jendso/bvaa046.2312

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