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Congenital generalized lipodystrophy type 2

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Description

Berardinelli-Seip congenital lipodystrophy (BSCL) is usually diagnosed at birth or soon thereafter. Because of the absence of functional adipocytes, lipid is stored in other tissues, including muscle and liver. Affected individuals develop insulin resistance and approximately 25%-35% develop diabetes mellitus between ages 15 and 20 years. Hepatomegaly secondary to hepatic steatosis and skeletal muscle hypertrophy occur in all affected individuals. Hypertrophic cardiomyopathy is reported in 20%-25% of affected individuals and is a significant cause of morbidity from cardiac failure and early mortality.

GeneReviews

  • Mode of Inheritance

  • Heterogeneous
  • Autosomal recessive inheritance

VARIANTS

55

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Genes

External Links

  • OMIM

    269700

  • Orphanet
  • HPO
  • Medgen

    C1720863

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