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chylomicronFood
plasmaMilitary unit
lipoprotein lipasePerson
autosomal recessiveDisease
triglycerideChemical compound
lipoproteinLegislature
eruptive xanthomaDisease
Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder of lipoprotein metabolism. It is characterized by marked elevation of triglyceride and chylomicron levels, lipaemic plasma, recurrent pancreatitis, eruptive xanthoma, hepatosplenomegaly, andliapemiaretinalis. All genes associated with FCS (LPL, APOC2, APOA5, LMF1 and GPHBP1) have an effect on the activity of lipoprotein lipase (LPL). The aim of this study is to present all cases with FCS clinical diagnosis, studied in our laboratory.N/
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
OBJECTIVE: Familial chylomicronemia syndrome (FCS) and multifactorial chylomicronemia syndrome (MCS)...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Aim: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder of lipoprotein ...
Familial Chylomicronemia Syndrome (FCS) is a rare autosomal recessive lipid disorder characterized b...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
International audiencePurpose of Review Familial chylomicronemia syndrome (FCS) is a rare recessive ...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronemia syndrome (FCS) is a rare metabolic disorder caused by mutations in lipoprot...
Familial chylomicronemia syndrome (FCS) is a rare and severe genetic disorder, characterized by mark...
BACKGROUND Familial chylomicronemia syndrome (FCS) is an ultra-rare phenotype that is usually cau...
Background: Familial chylomicronemia syndrome (FCS) is an ultra-rare phenotype that is usually cause...
Background Familial chylomicronemia syndrome (FCS) is a rare genetic disease that leads to severe hy...
Familial chylomicronemia syndrome (FCS) is caused by homozygous or compound heterozygous mutations i...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
OBJECTIVE: Familial chylomicronemia syndrome (FCS) and multifactorial chylomicronemia syndrome (MCS)...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Aim: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder of lipoprotein ...
Familial Chylomicronemia Syndrome (FCS) is a rare autosomal recessive lipid disorder characterized b...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
International audiencePurpose of Review Familial chylomicronemia syndrome (FCS) is a rare recessive ...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronemia syndrome (FCS) is a rare metabolic disorder caused by mutations in lipoprot...
Familial chylomicronemia syndrome (FCS) is a rare and severe genetic disorder, characterized by mark...
BACKGROUND Familial chylomicronemia syndrome (FCS) is an ultra-rare phenotype that is usually cau...
Background: Familial chylomicronemia syndrome (FCS) is an ultra-rare phenotype that is usually cause...
Background Familial chylomicronemia syndrome (FCS) is a rare genetic disease that leads to severe hy...
Familial chylomicronemia syndrome (FCS) is caused by homozygous or compound heterozygous mutations i...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
OBJECTIVE: Familial chylomicronemia syndrome (FCS) and multifactorial chylomicronemia syndrome (MCS)...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
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