• Title of article

    Congenital Generalized Lipodystrophy in a Youth Presented with Sclerotic and Lytic Bone Lesions; a Family with AGPAT2 Mutation

  • Author/Authors

    Hasani-Ranjbar, Shirin Obesity and Eating Habits Research Center - Endocrinology and Metabolism Molecular-Cellular Sciences Institute - Tehran University of Medical Sciences, Iran , Soltani, Akbar Endocrinology and Metabolism Research Center - Endocrinology and Metabolism Clinical Sciences Institute - Tehran University of Medical Sciences, Iran , Hadavi, Marzieh Endocrinology and Metabolism Research Center - Endocrinology and Metabolism Clinical Sciences Institute - Tehran University of Medical Sciences, Iran , Ejtahed, Hanieh-Sadat Obesity and Eating Habits Research Center - Endocrinology and Metabolism Molecular-Cellular Sciences Institute - Tehran University of Medical Sciences, Iran , Amoli, Mohammad Metabolic Disorders Research Center - Endocrinology and Metabolism Molecular-Cellular Sciences Institute - Tehran University of Medical Sciences, Iran , Radmard, Amir Reza Department of Radiology - Shariati Hospital, University of Medical Sciences, Tehran, Iran

  • Pages
    10
  • From page
    4275
  • To page
    4284
  • Abstract
    Background Congenital 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 Presentation We 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. Conclusion The young female had acral enlargement, hepatomegaly and both sclerotic and cystic bone lesions with AGPAT2 mutation.
  • Keywords
    AGPAT2 mutation , Congenital generalized lipodystrophy , Cystic bone lesions
  • Journal title
    International Journal of Pediatrics
  • Serial Year
    2017
  • Record number

    2521424