[Difficult to manage diabetes mellitus associated with generalized congenital lipodystrophy. Report of two cases]

An Pediatr (Barc). 2011 Feb;74(2):126-30. doi: 10.1016/j.anpedi.2010.09.020. Epub 2010 Dec 17.
[Article in Spanish]

Abstract

Generalized congenital lipodystrophy or Berardinelli-Seip Syndrome is a rare autosomal recessive condition characterized by the absence of adipose tissue and eventually a defect in leptin synthesis. Affected subjects tend to show a classical phenotype with acromegaloid appearance, generalized atrophy of subcutaneous adipose tissue with muscular hypertrophy, acanthosis nigricans, hepatomegaly and prominent abdomen. From metabolic point of view and as a consequence of leptin absence, hypertriglyceridemia leading to hepatic steatosis and insulin resistance may appear. Two cases of unrelated subjects affected of generalized congenital lipodystrophy are presented. Both developed difficult-to-manage diabetes mellitus and were treated with high doses of insulin. In both cases early microvascular complications were present. A mutation for LMNA gene was found in one of the subjects.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Adolescent
  • Child
  • Diabetes Complications / drug therapy*
  • Diabetes Mellitus / drug therapy*
  • Female
  • Humans
  • Lipodystrophy, Congenital Generalized / complications*
  • Male