Congenital Generalized Lipodystrophy Type 1

Known as: Lipodystrophy, Congenital Generalized, Type 1, Berardinelli Seip Congenital Lipodystrophy Type 1, Brunzell Syndrome, AGPAT2-Related 
It is caused by mutations of gene encoding 1-acylglycerol-3-phosphate O-acyltransferase-2 (AGPAT2).
National Institutes of Health

Topic mentions per year

Topic mentions per year

1984-2016
02419842016

Papers overview

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2012
2012
Congenital generalized lipodystrophy (CGL) is an autosomal recessive disease characterized by the generalized scant of adipose… (More)
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2010
2010
Congenital generalized lipodystrophy (CGL), characterized by generalized absence of adipose tissue, has heterogeneous causes… (More)
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2008
2008
Congenital generalized lipodystrophy type 1 (CGL-1) is characterized by an absence of adipose tissue and decreased serum leptin… (More)
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2008
2008
Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by extreme paucity of adipose… (More)
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2008
2008
We compare three Arabidopsis (Arabidopsis thaliana) complex glycan1 (cgl1) alleles and report on genetic interaction with… (More)
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2003
2003
Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive syndrome characterized by extreme paucity of adipose… (More)
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Highly Cited
2002
Highly Cited
2002
Generalised lipodystrophy of the Berardinelli-Seip type (BSCL) is a rare autosomal recessive human disorder with severe adverse… (More)
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Highly Cited
2001
Highly Cited
2001
Congenital generalized lipodystrophy, or Berardinelli–Seip syndrome (BSCL), is a rare autosomal recessive disease characterized… (More)
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Highly Cited
1999
Highly Cited
1999
Congenital generalized lipodystrophy (CGL, Berardinelli-Seip Syndrome, OMIM # 269700) is a rare autosomal recessive disorder… (More)
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1996
1996
BACKGROUND Atopy is a common syndrome underlying asthma, rhinitis, and eczema, and is characterised by high immunoglobulin E (IgE… (More)
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