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  • 标题:Congenital Generalized Lipodystrophy in a Youth Presented with Sclerotic and Lytic Bone Lesions; a Family with AGPAT2 Mutation
  • 本地全文:下载
  • 作者:Shirin Hasani-Ranjbar ; Akbar Soltani ; Marzieh Hadavi
  • 期刊名称:International Journal of Pediatrics
  • 印刷版ISSN:2345-5047
  • 电子版ISSN:2345-5055
  • 出版年度:2017
  • 卷号:5
  • 期号:2
  • 页码:4275-4284
  • DOI:10.22038/ijp.2016.7849
  • 语种:English
  • 出版社:Mashhad University of Medical Sciences
  • 其他摘要:BackgroundCongenital generalized lipodystrophy (CGL) is a rare disease. It is associated with near total fat loss, severe insulin resistance and hypoleptinemia leading to metabolic derangements.Case PresentationWe report a 25- year- old female with 1-Acylglycerol-3-phosphate-O-acyltransferase 2 (APGAT2) mutation, and both sclerotic and lytic bone lesions together for the first time. Bone cyst is one of the manifestations of CGL with AGPAT2 mutation. Patients usually have sclerotic bone lesions before and lytic bone lesions after puberty. Our patient had lytic bone lesions in (femur) long bones and also sclerotic lesions in the pelvic which was related to AGPAT2 mutation.ConclusionThe young female hadacral enlargement, hepatomegaly and both sclerotic and cystic bone lesions with AGPAT2 mutation.
  • 其他关键词:AGPAT2 mutation; Congenital generalized lipodystrophy; Cystic bone lesions
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