• By Ambry Genetics
  • Posted May 15, 2019

Familial Hypercholesterolemia: A Silent Threat That is too Often Missed

Familial hypercholesterolemia (FH) is an inherited genetic disorder characterized by markedly elevated low-density lipoprotein cholesterol (LDL-C) and accelerated atherosclerotic cardiovascular disease (ASCVD), leading to early heart attacks and heart disease. One of the most common genetic disorders, FH affects 1 in 250 individuals in the United…


  • By Andy Castro
  • Posted March 12, 2019

Food for Thought: Genetic Testing and the Fight Against Familial Hypercholesterolemia

Summer has arrived, and with it comes our seasonal obsession with barbecues, ice cream, and other less-than-healthy (but delicious, nonetheless) food options. Most of us will just be putting our beach bodies in jeopardy with our overindulgence, but for a large portion of the population, there will something much greater at stake: a significantly…


  • By Amanda Sheldon
  • Posted February 28, 2018

Finding the Missing Link of Heart Disease in Families: Familial Hypercholesterolemia (FH)

Many people have friends and family members who tell stories of losing their father when he was 40, or having a mother who had a heart attack in her 30s. These same people may even know that they have high cholesterol, and sometimes are told it is inherited. What they don’t know is that this condition could be familial hypercholesterolemia (FH)…


  • By Aaron Schmidt
  • Posted February 12, 2018

Science in 60 - Genetic Testing and Familial Hypercholesterolemia - (FH)

Editor’s Note: Science in 60 is a new video series from Ambry in which our researchers will give a brief overview of how genetic testing can help everyone understand disease. In this inaugural segment, Ambry genetic counselor Tami Johnston, MS CGC, looks at how genetic testing can improve the diagnoses and treatment plans for patients with