سامانه مدیریت نشریات علمی دانشگاه علوم پزشکی مشهد

Hasani-Ranjbar, Shirin, Soltani, Akbar, Hadavi, Marzieh, Ejtahed, Hanieh-Sadat, Mohammad-Amoli, Mahsa, Radmard, Amir Reza. (1395). Congenital Generalized Lipodystrophy in a Youth Presented with Sclerotic and Lytic Bone Lesions; a Family with AGPAT2 Mutation. , 5(2), 4275-4284. doi: 10.22038/ijp.2016.7849
Shirin Hasani-Ranjbar; Akbar Soltani; Marzieh Hadavi; Hanieh-Sadat Ejtahed; Mahsa Mohammad-Amoli; Amir Reza Radmard. "Congenital Generalized Lipodystrophy in a Youth Presented with Sclerotic and Lytic Bone Lesions; a Family with AGPAT2 Mutation". , 5, 2, 1395, 4275-4284. doi: 10.22038/ijp.2016.7849
Hasani-Ranjbar, Shirin, Soltani, Akbar, Hadavi, Marzieh, Ejtahed, Hanieh-Sadat, Mohammad-Amoli, Mahsa, Radmard, Amir Reza. (1395). 'Congenital Generalized Lipodystrophy in a Youth Presented with Sclerotic and Lytic Bone Lesions; a Family with AGPAT2 Mutation', , 5(2), pp. 4275-4284. doi: 10.22038/ijp.2016.7849
Hasani-Ranjbar, Shirin, Soltani, Akbar, Hadavi, Marzieh, Ejtahed, Hanieh-Sadat, Mohammad-Amoli, Mahsa, Radmard, Amir Reza. Congenital Generalized Lipodystrophy in a Youth Presented with Sclerotic and Lytic Bone Lesions; a Family with AGPAT2 Mutation. , 1395; 5(2): 4275-4284. doi: 10.22038/ijp.2016.7849

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

Journal of Pediatric Perspectives
مقاله 2، دوره 5، شماره 2 - شماره پیاپی 38، اردیبهشت 2017، صفحه 4275-4284    اصل مقاله (695.92 K)
شناسه دیجیتال (DOI): 10.22038/ijp.2016.7849
نویسندگان
Shirin Hasani-Ranjbar* 1؛ Akbar Soltani2؛ Marzieh Hadavi2؛ Hanieh-Sadat Ejtahed1؛ Mahsa Mohammad-Amoli3؛ Amir Reza Radmard4
1Obesity and Eating Habits Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
2Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
3Metabolic Disorders Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
4Department of Radiology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.
چکیده
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 hadacral enlargement, hepatomegaly and both sclerotic and cystic bone lesions with AGPAT2 mutation.
کلیدواژه‌ها
AGPAT2 mutation؛ Congenital generalized lipodystrophy؛ Cystic bone lesions
آمار
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