Cure My Disease

Don't miss your cure!

 Log in / Sign up

Familial partial lipodystrophy, Dunnigan type

MONDO:0007906

Familial Partial lipodystrophy, Dunnigan type (FPLD2) is a rare form of genetic lipodystrophy characterized by a loss of subcutaneous adipose tissue from the trunk, buttocks and limbs; fat accumulation in the neck, face, axillary and pelvic regions; muscular hypertrophy; and usually associated with metabolic complications such as insulin resistance, diabetes mellitus, dyslipidemia and liver steatosis.

Also known as: Dunnigan syndrome, FPLD2, familial partial lipodystrophy type 2, FPL2, lipodystrophy, familial partial, Dunnigan type, lipodystrophy, familial partial, type 2, lipodystrophy, familial, of limbs and Lower trunk, lipodystrophy, reverse partial

37 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 5 Not yet finished but already full! 4 Completed 8
Sort by