Cure My Disease

Don't miss your cure!

 Log in / Sign up

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

35 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Skin disorder (123) Inborn errors of metabolism (42) Lipodystrophy (26) Human disease (14) Familial partial lipodystrophy (11) Partial lipodystrophy (6) Hereditary skin disorder (5)
Trials to join now! 20 Not yet recruiting 4 Not yet finished but already full! 4 Completed 7
Sort by