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New routes to clinical diagnosis of FCS

This paper explores the way in which clinical results can separate patients with FCS from patients with severe hypertriglyceridaemia – important when advising on treatment options and where genetic testing is hard to come by, or is very slow.   Differentiating Familial Chylomicronaemia Syndrome from Multifactorial Severe Hypertriglyceridemia by Clinical Profile : Louis St L O’Dea, James […]

This paper explores the way in which clinical results can separate patients with FCS from patients with severe hypertriglyceridaemia – important when advising on treatment options and where genetic testing is hard to come by, or is very slow.

 

Differentiating Familial Chylomicronaemia Syndrome from Multifactorial Severe Hypertriglyceridemia by Clinical Profile : Louis St L O’Dea, James MacDougall, Veronica J Alexander, Andres Digenio, Brant Hubbard, Marcello Arca, Patrick M Moriarty, John J P Kastelein, Eric Bruckert, Handrean Soran, Joseph L Witztum, Robert A Hegele, Daniel Gaudet