Familial partial lipodystrophy

Known as: Familial Partial Lipodystrophies, Koberling Dunnigan Syndrome, Partial Lipodystrophy, Familial 
Inherited conditions characterized by the partial loss of ADIPOSE TISSUE, either confined to the extremities with normal or increased fat deposits on… (More)
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Lipodystrophic syndromes are characterized by adipose tissue deficiency. Although rare, they are of considerable interest as they… (More)
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2005
2005
OBJECTIVES:Characterization of familial clusters of subjects with metabolic derangements predisposing to hepatic steatosis and… (More)
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2003
2003
OBJECTIVE The phenotypic expression of partial lipodystrophy is present in two familial syndromes: familial partial lipodystrophy… (More)
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Highly Cited
2002
Highly Cited
2002
Autosomal dominant familial partial lipodystrophy (FPLD) due to mutant LMNA encoding nuclear lamin A/C is characterized by… (More)
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Highly Cited
2002
Highly Cited
2002
Familial partial lipodystrophies (FPL) are a heterogeneous group of genetic disorders characterized by marked loss of… (More)
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Highly Cited
2002
Highly Cited
2002
The gene encoding nuclear lamins A and C is mutated in at least three inherited disorders. Two of these, Emery-Dreifuss muscular… (More)
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Highly Cited
2002
Highly Cited
2002
Lipodystrophies are characterized by selective but variable loss of body fat and metabolic complications of insulin resistance… (More)
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Highly Cited
2000
Highly Cited
2000
Patients with Dunnigan-type familial partial lipodystrophy (FPLD) are born with normal fat distribution, but after puberty… (More)
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Highly Cited
2000
Highly Cited
2000
Familial partial lipodystrophy (FPLD), Dunnigan variety, is an autosomal dominant disorder characterized by marked loss of… (More)
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Highly Cited
1999
Highly Cited
1999
Familial partial lipodystrophy, Dunnigan type (FPLD), is a rare autosomal dominant genetic disorder characterized by gradual loss… (More)
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