نتایج جستجو برای: Congenital generalized lipodystrophy

تعداد نتایج: 286938  

Journal: :گوارش 0
simin partovi davoud sharifi hamid khalesi

congenital generalized lipodystrophy (cgl) is a rare and progressive disorder (1 in 12 milion). common clinical manifestations are lipoatrophy, acromegaloid feature, acanthosis nigricans, hyperlipidemia, diabetes mellitus or abnormal glucose tolerance test.â rarely fatty liver and cirrhosis is seen. the highest number reported in literature is 8 cases from brazil and 6 cases from scandinavia, r...

Journal: :Jornal de Pediatria 2004

Journal: :international journal of pediatrics 0
shirin hasani-ranjbar obesity and eating habits research center, endocrinology and metabolism molecular-cellular sciences institute, tehran university of medical sciences, tehran, iran. akbar soltani endocrinology and metabolism research center, endocrinology and metabolism clinical sciences institute, tehran university of medical sciences, tehran, iran. marzieh hadavi endocrinology and metabolism research center, endocrinology and metabolism clinical sciences institute, tehran university of medical sciences, tehran, iran. hanieh-sadat ejtahed obesity and eating habits research center, endocrinology and metabolism molecular-cellular sciences institute, tehran university of medical sciences, tehran, iran. mahsa mohammad-amoli metabolic disorders research center, endocrinology and metabolism molecular-cellular sciences institute, tehran university of medical sciences, tehran, iran. amir reza radmard department of radiology, shariati hospital, tehran university of medical sciences, tehran, iran.

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 i...

Journal: :Jornal de pediatria 2004
Paulo P Figueiredo Filho Alexandre Costa Val Rosângela Diamante Cristiane F Cunha Rocksane C Norton Joel A Lamounier Ennio Leão

OBJECTIVE To present the major clinical and biochemical characteristics of congenital generalized lipodystrophy. DESCRIPTION Eight infants with congenital generalized lipodystrophy were identified at the Endocrine and Nutritional Pediatric Disease Outpatient Clinics at Hospital de Clínicas, Universidade Federal de Minas Gerais (UFMG). Clinical manifestations common to all patients included mu...

Journal: :Journal of the Formosan Medical Association 2019

Journal: :JPMA. The Journal of the Pakistan Medical Association 1992
N Jafri Z Zaidi

Clinical features of congenital generalized lipodystrophy, a rare disorder, first described by Zeigler include loss of subcutaneous fat, hepatomegaly, increased bone growth, hyperlipaemia and, later, diabetes. The inheritance is probably autosomal recessive. Generalized lipodystrophy may involve the diencephalon. A probable defect in the hypothalamus may lead to increased levels of hypothalamic...

2015
Shafeek A. Mulla Ghazala A. Farooqi Abdul Aziz Al- Rashed

Congenital generalized lipodystrophy (GLD) is a rare autosomal recessive disease characterized by near absence of adipose tissue from birth or early infancy and severe insulin resistance. Since Berardinelli described a very rare case of congenital generalized lipodystrophy, nearly 120 cases have been reported in the literature. We report a case of GLD which, to the best of our knowledge, is the...

Journal: :genetics in the 3rd millennium 0
pooneh nikuei kianoosh malekzadeh minoo rajaei yousef shafeghati

congenital generalized lipodystrophies (cgls) are very rare autosomal recessive disorders which have four types.of the four cgl types, bscl2 (berardinelli–seip congenital lipodystrophy type 2) is the result of mutations in the bscl2/seipingene.bscl2 which is the most severe lipodystrophic phenotype is characterized by generalized lipodystrophy, overgrowth,acanthosisnigricans, hepatomegaly, insu...

Journal: :Diagnostic and interventional radiology 2017
Canan Altay Mustafa Seçil Tevfik Demir Tahir Atik Gülçin Akıncı Nilüfer Özdemir Kutbay Ela Keskin Temeloğlu Ilgın Yıldırım Şimşir Seçil Özışık Leyla Demir Erdal Eren Emine Burçin Tuna Hasibe Aytaç Hüseyin Onay Barış Akıncı

PURPOSE We aimed to investigate residual adipose tissue with whole-body magnetic resonance imaging to differentiate between subtypes of lipodystrophy. METHODS A total of 32 patients (12 with congenital generalized lipodystrophy [CGL], 1 with acquired generalized lipodystrophy [AGL], 12 with familial partial lipodystrophy [FPLD], and 7 with acquired partial lipodystrophy [APL]) were included. ...

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