Display Settings:

Format

Send to:

Choose Destination
See comment in PubMed Commons below
Ann Endocrinol (Paris). 2013 Feb;74(1):59-61. doi: 10.1016/j.ando.2012.11.008. Epub 2013 Jan 18.

AGPAT2 gene mutation in a child with Berardinelli-Seip congenital lipodystrophy syndrome.

Author information

  • 1Department of pediatric endocrinology, Children's medical center, Tehran university of medical sciences, Tehran, Iran.

Abstract

Berardinelli-Seip congenital lipodystrophy (BSCL) syndrome is an autosomal recessive disorder, caused by mutation in the AGPAT2 gene, which could lead to insulin resistance and variety of complications. Herein, a 7-year old girl is presented with generalized loss of subcutaneous fat, prominent pectoral and thigh muscles and an early telarche. Laboratory studies revealed an elevated level of serum triglyceride. Ultrasonograph demonstrated enhanced size of ovary containing multiple mature follicles. Considering the clinical phenotype, AGPAT2 gene was sequenced which showed homozygote c.514G>A mutation. Therefore, the diagnosis of BSCL was confirmed in this patient.

Copyright © 2012 Elsevier Masson SAS. All rights reserved.

PMID:
23337016
[PubMed - indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Icon for Masson (France)
    Loading ...
    Write to the Help Desk