Genetic testing may aid in diagnosing familial chylomicronemia syndrome (FCS)4

A diagnosis supported by genetic testing can guide recommendations, management strategies, and referrals

For those presenting with the clinical characteristics of FCS, multi-gene panels search for functional mutations in the genes essential to LPL function.4

The FCS genetic testing program 

Sponsored by Ionis Pharmaceuticals, genetic testing is available to certain qualifying patients who have:

  • Extremely high triglyceride levels (>880 mg/dL or >10 mmol/L), on two fasting blood tests in a row.
  • No other known causes of high triglyceride levels.

As part of the program’s partnership, an independent genetic counseling service, Genome Medical, can provide information on FCS and support during the genetic testing process.

Call Genome Medical at +1 888.478.1494 to learn more.