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Familial partial lipodystrophy, Kobberling type

MONDO:0012072

Familial partial lipodystrophy, Kobberling type, is a very rare form of familial partial lipodystrophy (FPLD) of unknown etiology characterized by lipoatrophy that is confined to the limbs and a normal or increased fat distribution of the face, neck, and trunk. Arterial hypertension and diabetes have also been associated. Inheritance is thought to be autosomal dominant.

Also known as: FPLD1, familial partial lipodystrophy type 1, familial partial lipodystrophy type Köbberling, familial partial lipodystrophy, Köbberling type, lipodystrophy, familial partial, Kobberling type, lipodystrophy, familial partial, type 1

5 clinical trials for this condition and its sub-types, 0 tagged with Familial partial lipodystrophy, Kobberling type itself.

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