Cardiology - FAMILION®
Transgenomic FAMILION Tests
The FAMILION tests detect genetic mutations that can cause cardiac channelopathies, cardiomyopathies and other cardiopathies. For patients suspected of having an inherited cardiac disease, genetic testing may help:
Confirm the diagnosis- Provide valuable risk stratification information
- Guide treatment decisions
- Identify presymptomatic or silent carriers
- Enable better genetic counseling
Transgenomic Patient Services – Helping Families Everyday
Our experienced team works to help your patients navigate the healthcare insurance environment. Our goal is to minimize the patient’s out-of-pocket expense. To learn more about how our Patients Services team and billing practices put patients first, click here.
Transgenomic Clinical Genetics Team – Helping Healthcare Professionals
With professional backgrounds in genetics and genetic counseling, the Transgenomic Clinical Genetics team is available for consultation about the FAMILION family of genetic tests. To contact our Clinical Genetics team with technical questions about FAMILION testing or to aid in interpreting test results, please email us at ClinicalGenetics [-- at --] transgenomic [dot] com.
| Marfan/TAAD | Marfan Syndrome and Familial TAAD (Marfan/TAAD) |
| Marfan Large Del/Dup | Marfan Syndrome Large Deletion/Duplication Test |
| Postmortem Cardiomyopathies |
| Postmortem Channelopathies |

