Development and validation of clinical criteria to identify familial chylomicronemia syndrome (FCS) in North America

Familial chylomicronemia syndrome (FCS) is an ultrarare inherited disorder. Genetic testing is not always feasible or conclusive. European clinicians developed a “FCS score” to differentiate between FCS and multifactorial chylomicronemia syndrome (MCS), a more common condition with overlapping featu...

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Veröffentlicht in:	Journal of clinical lipidology 2024-11
Hauptverfasser:	Hegele, Robert A., Ahmad, Zahid, Ashraf, Ambika, Baldassarra, Andrew, Brown, Alan S., Chait, Alan, Freedman, Steven D., Kohn, Brenda, Miller, Michael, Patni, Nivedita, Soffer, Daniel E., Wang, Jian, Broder, Michael S., Chang, Eunice, Yermilov, Irina, Campos, Cynthia, Gibbs, Sarah N
Format:	Artikel
Sprache:	eng
Schlagworte:	Delphi panel Familial chylomicronemia syndrome Hypertriglyceridemia Lipoprotein lipase deficiency Multifactorial chylomicronemia syndrome Pancreatitis
Online-Zugang:	Volltext
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