Indian Journal of Endocrinology and Metabolism (Jan 2012)

Body fat distribution in women with familial partial lipodystrophy caused by mutation in the lamin A/C gene

  • Luciana Z Monteiro,
  • Maria C Foss-Freitas,
  • Renan M Montenegro,
  • Milton C Foss

DOI
https://doi.org/10.4103/2230-8210.91209
Journal volume & issue
Vol. 16, no. 1
pp. 136 – 138

Abstract

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Familial partial lipodystrophy (FPLD), Dunnigan variety, is an autosomal dominant disorder caused due to missense mutations in the lamin A/C (LMNA) gene encoding nuclear lamina proteins. Patients with FPLD are predisposed to metabolic complications of insulin resistance such as diabetes. We sought to evaluate and compare body fat distribution with dual-emission X-ray absorptiometry in women with and without FPLD and identify densitometric, clinical and metabolic features.

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