نتایج جستجو برای: berardinelli

تعداد نتایج: 127  

2017
Lázaro Batista de Azevedo Medeiros Verônica Kristina Cândido Dantas Aquiles Sales Craveiro Sarmento Lucymara Fassarella Agnez-Lima Adriana Lúcia Meireles Thaiza Teixeira Xavier Nobre Josivan Gomes de Lima Julliane Tamara Araújo de Melo Campos

BACKGROUND Berardinelli-Seip Congenital Lipodystrophy (BSCL) is a rare disease characterized by the almost complete absence of adipose tissue. Although a large number of BSCL cases was previously identified in Rio Grande do Norte (RN), a state in Northeast Brazil, its prevalence in RN regions and municipalities remains unknown. The purpose of this study was to better characterize the prevalence...

2015
Caroline Schnoll Erika Bezerra Parente Paula Vieira Freire Ibrahim Ahmad H El Bacha Edison Roberto Parise Joao Eduardo Nunes Salles

Results Patients 1 and 3 were diagnosed late, by the age of 54 and 43 yrs. respectively. While the second patient was diagnosed earlier at 17th and follows 14 yrs. in treatment. All patients have low body fat on DEXA (Figure 1) and moderate steatosis, but only the Patient 2 has no fibrosis. The patients’ metabolic profile after the treatment is exposed at Table 1. All patients are in use, at le...

Journal: :Diabetes 2002
Kirsten Heathcote Anna Rajab Jocelyne Magré Petros Syrris Mehran Besti Michael Patton Marc Délépine Mark Lathrop Jacqueline Capeau Steve Jeffery

Congenital generalized lipodystrophy (CGL) is a rare disorder characterized by the absence of body fat and insulin resistance and accompanied by other features, including acanthosis nigricans, organomegaly, hyperandrogenism, and diabetes. We have examined case subjects from 11 families in Oman with CGL. All subjects were the progeny of consanguineous marriages; therefore, a homozygosity mapping...

2016
L. Dollet J. Magré M. Joubert C. Le May A. Ayer L. Arnaud C. Pecqueur V. Blouin B. Cariou X. Prieur

Loss-of-function mutations in BSCL2 are responsible for Berardinelli-Seip congenital lipodystrophy, a rare disorder characterized by near absence of adipose tissue associated with insulin resistance. Seipin-deficient (Bscl2-/-) mice display an almost total loss of white adipose tissue (WAT) with residual brown adipose tissue (BAT). Previous cellular studies have shown that seipin deficiency alt...

Journal: :Diabetes 2003
Jocelyne Magré Marc Delépine Lionel Van Maldergem Jean-Jacques Robert J Antonie Maassen Muriel Meier Vanessa R Panz Chong Ae Kim Nadia Tubiana-Rufi Paul Czernichow Eva Seemanova Charles R Buchanan Didier Lacombe Corinne Vigouroux Olivier Lascols C Ronald Kahn Jacqueline Capeau Mark Lathrop

Berardinelli-Seip congenital lipodystrophy (BSCL) is a heterogeneous genetic disease characterized by near absence of adipose tissue and severe insulin resistance. We have previously identified mutations in the seipin gene in a subset of our patients' cohort. Recently, disease-causing mutations in AGPAT2 have been reported in BSCL patients. In this study, we have performed mutation screening in...

Journal: :Human molecular genetics 2013
Maarit Hölttä-Vuori Veijo T Salo Yuki Ohsaki Maximiliano L Suster Elina Ikonen

Mutations affecting the N-glycosylation site in Berardinelli-Seip lipodystrophy (BSCL)-associated gene BSCL2/seipin lead to a dominantly inherited spastic paraplegia termed seipinopathy. While the loss of function of seipin leads to severe congenital lipodystrophy, the effects of seipin N-glycosylation mutations on lipid balance in the nervous system are unknown. In this study, we show that exp...

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