Expert Video - What are the genetic factors for developing FCS?
Physicians describe the genetics of Familial Chylomicronemia Syndrome (FCS) and explain that it is a rare autosomal recessive disorder. If you have FCS, your family members or relatives may also have it, or they may carry one copy of the abnormal gene. People who have one abnormal gene are called carriers. They don’t have FCS, but if two carriers have a child together, there’s a one in four chance that the child will have FCS.
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Other Sections in this Module:
Animation - Understanding FCS
Slide Show - Understanding FCS
1.
What is FCS?
2.
What are chylomicrons?
3.
What causes FCS?
4.
What are the signs and symptoms of FCS?
5.
Why is the pancreas involved in FCS?
6.
What are the genetic factors for developing FCS?
7.
What challenges do people with FCS face?
8.
What type of low fat diet should FCS patients follow?
9.
Can patients with FCS drink alcohol or smoke tobacco?
10.
What risks do women with FCS face if they become pregnant?
11.
How is Familial Chylomicronemia Syndrome (FCS) treated?
12.
What resources and networks are available to FCS patients?
