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2287 ECG and echo characteristics in familial partial lipodystrophy: The impact of Lamin A variants

OBJECTIVES/SPECIFIC AIMS: Familial partial lipodystrophy (FPLD) is an inherited, rare syndrome characterized by selective absence of adipose tissue from extremities which is associated with severe insulin resistance, and metabolic dyslipidemia (with hypertriglyceridemia, and low HDL) Typically, 30%–...

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Publicat a:J Clin Transl Sci
Autors principals: Eldin, Abdelwahab J., Meral, Rasimcan, Neidert, Adam H., Rus, Diana, Hench, Rita, Oral, Hakan, Oral, Elif A.
Format: Artigo
Idioma:Inglês
Publicat: Cambridge University Press 2018
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6798885/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/cts.2018.164
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