Ärftliga sjukdomstillstånd som kännetecknas av partiell förlust av fettvävnad, antingen begränsad till extremiteterna, med normala eller ökade fettmängder i ansikte, hals och bål (typ 1), eller begränsad till förlust av underhudsfett på lemmar och bål (typ 2).
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.
Koberling-Dunnigans syndrom — Familjär partiell lipodystrofi, typ 2 — Dunnigans syndrom — Familjär partiell lipodystrofi, typ 3 — Familjär partiell lipodystrofi, typ 1
Familial Partial Lipodystrophies — Partial Lipodystrophy, Familial — Familial Partial Lipodystrophy — Koberling-Dunnigan Syndrome — Koberling Dunnigan Syndrome — Familial Partial Lipodystrophy, Type 2 — Lipodystrophy, Familial, of Limbs and Lower Trunk — Lipodystrophy, Familial Partial, Dunnigan Type — Lipodystrophy, Reverse Partial — Partial Lipodystrophies, Reverse — Partial Lipodystrophy, Reverse — Reverse Partial Lipodystrophies — Reverse Partial Lipodystrophy — Dunnigan Syndrome — Lipodystrophy, Familial Partial, Type 2 — Familial Partial Lipodystrophy, Type 3 — Lipodystrophy, Familial Partial, Associated With PPARg Mutations — Lipodystrophy, Familial Partial, Type 3 — Familial Partial Lipodystrophy, Type 1 — Familial Partial Lipodystrophy, Kobberling Type — Lipodystrophy, Familial Partial, Kobberling Type — Lipodystrophy, Familial Partial, Type 1