Rare Diagnosis of Familial Partial Lipodystrophy in a Patient With Life-Threatening Pancreatitis due to Hypertriglyceridemia

BACKGROUND: Familial partial lipodystrophy type 2 (FPLD2) is a rare genetic condition characterized by partial lack of subcutaneous tissue and can predispose an individual to complications such as hypertriglyceridemia with pancreatitis, insulin resistance, and diabetes. This report describes a case...

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Detalles Bibliográficos
Autores principales: Akamnonu, Chukwuka, Ueda, Masako, Shah, Ankit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association of Clinical Endocrinology 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784711/
https://www.ncbi.nlm.nih.gov/pubmed/35097194
http://dx.doi.org/10.1016/j.aace.2021.06.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784711/
https://www.ncbi.nlm.nih.gov/pubmed/35097194
http://dx.doi.org/10.1016/j.aace.2021.06.005

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