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Familial partial lipodystrophy
MONDO:0020088Familial partial lipodystrophy (FPLD) is a group of rare genetic lipodystrophic syndromes characterized, in most cases, by fat loss from the limbs and buttocks, from childhood or early adulthood, and often associated with acanthosis nigricans, insulin resistance, diabetes, hypertriglyceridemia and liver steatosis.
Also known as: FPLD, congenital partial lipodystrophy, genetic partial lipodystrophy, lipodystrophy, familial partial
45 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Familial partial lipodystrophy, Dunnigan type
(2)
AKT2-related familial partial lipodystrophy
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Autosomal semi-dominant severe lipodystrophic laminopathy
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CIDEC-related familial partial lipodystrophy
(0)
Familial partial lipodystrophy, Kobberling type
(0)
LIPE-related familial partial lipodystrophy
(0)
Lipodystrophy, familial partial, type 8
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Lipodystrophy, familial partial, type 9
(0)
PLIN1-related familial partial lipodystrophy
(0)
PPARG-related familial partial lipodystrophy
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