Fitting the pieces of the puzzle together: A case report of the Dunnigan-type of familial partial lipodystrophy in the adolescent girl

Familial partial lipodystrophy of the Dunnigan type (FPLD 2) is a rare autosomal dominant disorder caused by the mutations of the lamin A/C gene leading to the defective adipogenesis, premature death of adipocytes and lipotoxicity.