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Familial partial lipodystrophy, Dunnigan type

rare

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.

Causal genes
LMNA
Also known as
Dunnigan syndrome · familial partial lipodystrophy type 2 · FPL2 · FPLD2 · lipodystrophy, familial partial, type 2

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