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lipodystrophy, familial partial, type 2 (Dunnigan type) (FPLD2, LDHCP); lipoatrophic diabetes
Pathology:
- generalized lipoatrophy
- metabolic alterations
- massive liver steatosis
- cardiac abnormalities involving both endocardium & myocardium
Genetics:
- associated with defects in LMNA
Clinical manifestations:
- distinctive cutaneous manifestations
General
lipodystrophy; lipoatrophy
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 608056
References
OMIM :accession 608056