Same disease, different testing approaches: global survey highlights the need for standardized FH genetic testing
Familial hypercholesterolemia (FH) is a common inherited disorder affecting approximately 1 in 250...
In this webinar, Prof. Albert Wiegman (MD, PhD), paediatric cardiologist at Amsterdam UMC, talks about how early paediatric screening and genetic testing can guide detection and treatment of familial hypercholesterolemia (FH).
Currently, FH is diagnosed later in life at an median age of 44. In the webinar, Prof. Wiegman details how early cholesterol screening and genetic testing in children can improve patient outcomes and provide a cost-effective treatment strategy.
Familial hypercholesterolemia (FH) is a common inherited disorder affecting approximately 1 in 250...
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Meet Silvia Borras, a Development Lead and Clinical Scientist in Genetics and Molecular Pathology...
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