Condition 101 content is not available at this time, but we are continually updating the site. Please check back.

However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.

  • Condition: Familial Chylomicronemia Syndrome due to Heterozygous Deletion of Chromosome 8
  • Journal: Medicine
  • Treatment Used: Volanesorsen
  • Number of Patients: 1
  • Published —
This case report describes a 52-year-old woman with familial chylomicronemia syndrome due to a heterozygous deletion of the chromosome 8 treated with volanesorsen.
  • Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
  • Published —
THE PREVALENCE OF PROBABLE FAMILIAL CHYLOMICRONEMIA SYNDROME IN A SOUTHERN CALIFORNIA POPULATION.