Familial partial lipodystrophy 2 (FPLD2), or Dunnigan variety lipodystrophy, is an autosomal dominantly inherited condition that results from pathogenic variants in the LMNA gene,2, 3, 4, 5 located on chromosome 1q21.6, 7. Here, LMNA is linked to familial partial lipodystrophy, Dunnigan type.