Familial partial lipodystrophy, Dunnigan type

Orpha code: 2348OMIM code: 151660

Definition

A rare, 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.

Disease data
Classification

Disease

Synonyms
Dunnigan syndrome
Rodzinna lipodystrofia częściowa typu 2
Zespół Dunnigana
FPLD2
Familial partial lipodystrophy type 2
ORPHA code
2348
OMIM code
151660
ICD10 code
E88.1
ICD11 code
5A44

No additional description.

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