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Indian Pediatrics

, Volume 56, Issue 10, pp 877–878 | Cite as

Berardinelli Seip Congenital Lipodystrophy Syndrome: 10 Year Follow-up

  • Rajesh Joshi
  • Shreya SharmaEmail author
Clinical Case Letters
  • 14 Downloads

Abstract

Lipodystrophy syndromes are extremely rare disorders of deficient body fat associated with potentially serious metabolic complications. Here, we describe a 10-year-old girl with genetically proven Berardinelli Seip congenital generalized lipodystrophy type 2, diagnosed at 10 months of age. She developed comorbidities like proteinuria, hypertension, diabetes mellitus, and liver fibrosis.

Keywords

Insulin resistance Metabolic syndrome Liver fibrosis 

Notes

Funding: None; Competing interest: None stated.

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Copyright information

© Indian Academy of Pediatrics 2019

Authors and Affiliations

  1. 1.Division of Pediatric EndocrinologyBai Jerbai Wadia Hospital for ChildrenMumbaiIndia

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