Context: To date, all cases of familial partial lipodystrophy type 2 (FPLD2, MIM 151660) result from missense mutations in LMNA, which encodes for nuclear lamin A/C (MIM 150330).

Objective: To carry out mutational analysis of LMNA in two sisters with a particularly severe FPLD2 phenotype.

Design: Descriptive case report with molecular studies.

Setting: Referral Center.

Patients: We report two sisters of South Asian origin. The first presented with acanthosis nigricans at age 5 yr, diabetes with insulin resistance, hypertension and hypertriglyceridemia at age 13 yr and partial lipodystrophy starting at puberty. Her sister and their mother had a similar metabolic profile and physical features, and their mother died of vascular disease at age 32.

Interventions: None.

Main outcome measures and results: LMNA sequencing showed that the sisters were each heterozygous for a novel G>C mutation at the intron 8 consensus splice donor site, which was absent from the genomes of 300 healthy individuals. The retention of intron 8 in mRNA predicted a prematurely truncated lamin A isoform (516 instead of 664 amino acids) with 20 nonsense 3'-terminal residues. The mutant lamin A isoform failed to interact normally with emerin and failed to localize to the nuclear envelope.

Conclusions: This is the first LMNA splicing mutation to be associated with FPLD2, and it causes a severe clinical and metabolic phenotype.