TRYNGOLZA® (Olezarsen) Recommended for Approval in the EU by CHMP for Familial Chylomicronemia Syndrome (FCS)
Summary by The Huntsville Item
2 Articles
2 Articles
Living with Familial Chylomicronemia Syndrome – Patient Worthy
I live with a rare, genetic disease called familial chylomicronemia syndrome, or FCS, which prevents my body from breaking down fats and removing triglycerides from my bloodstream. FCS is inherited in an autosomal recessive manner, which means one has to inherit a mutated gene from both parents in order to “get” FCS. So, if both […]
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Leaning Left1Leaning Right0Center0Last UpdatedBias Distribution100% Left
Bias Distribution
- 100% of the sources lean Left
100% Left
L 100%
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