NIH GARD Information: Familial partial lipodystrophy associated with PLIN1 mutations
This information is provided by the National Institutes of Health (NIH)
Genetic and Rare Diseases Information Center (GARD).
- PLIN1-related familial partial lipodystrophy
- PLIN1-related FPLD
- Familial partial lipodystrophy type 4
- Lipodystrophy, familial partial, type 4
- FPLD due to PLIN1 mutations
No overview is available at this time. Please check back for future updates.
For more information, visit GARD.