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Familial Partial Lipodystrophy: A Case Study and Review of Recent Literature

Introduction: Familial partial lipodystrophy (FPLD) is a rare genetic disorder characterized by loss of subcutaneous adipose tissue, mainly from the extremities and gluteal region. FPLD is associated with a variety of metabolic abnormalities including severe hypertriglyceridemia (HTG), insulin resis...

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Detalles Bibliográficos
Autores principales:	Tipu, Ali, Hasan, Farhad, Grimes, Michael
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2021
Materias:	Cardiovascular Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265984/ http://dx.doi.org/10.1210/jendso/bvab048.629

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