نتایج جستجو برای: berardinelli

تعداد نتایج: 127  

Journal: :The Ceylon medical journal 2014
M P Senanayake I Karunaratne

Berardinelli-Seip congenital generalised lipodystrophy (BSCGL) is an extremely rare autosomal recessive disorder characterised by congenital absence of functional adipocytes causing lipoatrophy, dyslipidemia and fat maldistribution [1]. Fat deposited in liver, heart and muscle result in stetosis-induced cirrhosis, cardiac failure, insulin resistance and diabetes mellitus. We report two addition...

Journal: :Indian Dermatology Online Journal 2014

Journal: :Egyptian Journal of Medical Human Genetics 2015

Journal: :European journal of medical genetics 2009
B Friguls W Coroleu R del Alcazar P Hilbert L Van Maldergem G Pintos-Morell

Berardinelli-Seip congenital lipodystrophy (BSCL) is a rare autosomal recessive condition associating insulin resistance, absence of subcutaneous fat and muscular hypertrophy. Disease-causing mutations have been described in AGPAT2 and BSCL2 genes. Hypertrophic cardiomyopathy is a classical late (third decade) complication which has only been occasionally described in childhood. We report on a ...

Journal: :Palimpsesto - Revista do Programa de Pós-Graduação em Letras da UERJ 2019

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...

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