Lipodystrophy, Familial Partial
Inherited conditions characterized by the partial loss of ADIPOSE TISSUE, either confined to the extremities with normal or increased fat deposits on the face, neck and trunk (type 1), or confined to the loss of SUBCUTANEOUS FAT from the limbs and trunk (type 2). Type 3 is associated with mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA.
Year introduced: 2007
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Tree Number(s): C16.320.488.813, C17.800.849.391.700, C18.452.584.563.798, C18.452.584.625.700, C18.452.880.391.700
MeSH Unique ID: D052496
Entry Terms:
- Familial Partial Lipodystrophies
- Partial Lipodystrophy, Familial
- Koberling-Dunnigan Syndrome
- Koberling Dunnigan Syndrome
- Familial Partial Lipodystrophy
- Familial Partial Lipodystrophy, Type 2
- Dunnigan Syndrome
- Lipodystrophy, Familial Partial, Type 2
- Lipodystrophy, Familial Partial, Dunnigan Type
- Lipodystrophy, Reverse Partial
- Partial Lipodystrophies, Reverse
- Partial Lipodystrophy, Reverse
- Reverse Partial Lipodystrophies
- Reverse Partial Lipodystrophy
- Lipodystrophy, Familial, of Limbs and Lower Trunk
- Familial Partial Lipodystrophy, Type 1
- Lipodystrophy, Familial Partial, Type 1
- Familial Partial Lipodystrophy, Kobberling Type
- Lipodystrophy, Familial Partial, Kobberling Type
- Familial Partial Lipodystrophy, Type 3
- Lipodystrophy, Familial Partial, Type 3
- Lipodystrophy, Familial Partial, Associated With PPARg Mutations
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