EM2605F "Genetic and Acquired Lipodystrophies: Decoding Human Metabolism Through Rare Disorders" (IM GR-050826)
Purpose and Overview
To present the prevalence, clinical characteristics, metabolic derangements and molecular and autoimmune basis of genetic and acquired lipodystrophies. To review therapeutic optons for patients with lipodystrophies. To review implications of these rare disorders for patients with type 2 diabetes.
Target Audience
UT Southwestern faculty, fellows, residents and medical students, community physicians, nurse clinicians, physician assistants and nurses.
Learning Objectives
At the conclusion of this activity, the participant should be able to:
- Distinguish between the genetic and acquired lipodystrophies.
- Understand molecular genetic basis of congenital generalized and familial partial lipodystrophies.
- Learn therapeutic options for patients with lipodystrophies.

Abhimanyu Garg, M.D.
Professor of Internal Medicine
Division of Endocrinology
UT Southwestern Medical Center
Available Credit
- 1.00 AMA
Price
Required Hardware/software
Activities should be run with recent versions of common browsers, including Internet Explorer, Firefox and Google Chrome

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