Purpose of Review: Familial chylomicronemia syndrome (FCS) is a rare recessive genetic disorder often underdiagnosed with potentially severe clinical consequences. In this review, we describe the clinical and biological characteristics of the disease together with its main complication, i.e., acute pancreatitis. We focused the paper on new diagnostic tools, progress in understanding the role of two key proteins (apolipoprotein CIII (apo CIII) and angiopoietin-like3 (ANGPTL-3)), and new therapeutic options. Recent Findings: Recently, a new diagnostic tool has been proposed by European experts to help identify these patients. This tool with two recently identified parameters (low LDL and low body mass index) can help identify patients who sho...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
International audienceCONTEXT: The relative incidence of acute pancreatitis, ischemic cardiovascular...
International audiencePurpose of Review Familial chylomicronemia syndrome (FCS) is a rare recessive ...
Familial chylomicronemia syndrome (FCS) is a rare metabolic disorder caused by mutations in lipoprot...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronemia syndrome (FCS) is caused by homozygous or compound heterozygous mutations i...
International audienceBackground: Familial chylomicronemia syndrome (FCS) is a rare genetic disease ...
Aim: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder of lipoprotein ...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
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...
OBJECTIVE: Familial chylomicronemia syndrome (FCS) and multifactorial chylomicronemia syndrome (MCS)...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
International audienceCONTEXT: The relative incidence of acute pancreatitis, ischemic cardiovascular...
International audiencePurpose of Review Familial chylomicronemia syndrome (FCS) is a rare recessive ...
Familial chylomicronemia syndrome (FCS) is a rare metabolic disorder caused by mutations in lipoprot...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronemia syndrome (FCS) is caused by homozygous or compound heterozygous mutations i...
International audienceBackground: Familial chylomicronemia syndrome (FCS) is a rare genetic disease ...
Aim: Familial chylomicronemia syndrome (FCS) is a rare autosomal recessive disorder of lipoprotein ...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
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...
OBJECTIVE: Familial chylomicronemia syndrome (FCS) and multifactorial chylomicronemia syndrome (MCS)...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired cle...
International audienceCONTEXT: The relative incidence of acute pancreatitis, ischemic cardiovascular...