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

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

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 (APG...

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Bibliographic Details
Main Authors: Shirin Hasani-Ranjbar, Akbar Soltani, Marzieh Hadavi, Hanieh-Sadat Ejtahed, Mahsa Mohammad-Amoli, Amir Reza Radmard
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2017-02-01
Series:International Journal of Pediatrics
Subjects:
AGPAT2 mutation
Congenital generalized lipodystrophy
Cystic bone lesions
Online Access:http://ijp.mums.ac.ir/article_7849_bbe7b6e65b0f269ec19d9ed9aaf57cb4.pdf

Internet

http://ijp.mums.ac.ir/article_7849_bbe7b6e65b0f269ec19d9ed9aaf57cb4.pdf

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