Genetic Disease Diagnosis

Thrombophilia: Venous Thrombosis causes an estimated 50,000 deaths per year in the US and has an incidence of 1 per 1000 annually. There are many reported risk factors including a genetic element that can contribute to thrombosis. Cardiovascular disease is a leading cause of death for both men and women in most racial ethnic groups.

Alpha-1-Antitrypsin (AAT) deficiency: AAT deficiency is an autosomal recessive disorder that is virtually confined to Caucasians of European descent and is the most common genetic cause of liver disease in children and emphysema in adults.

Product Number	Kit Name	Notes
THF04B2	Elucigene TRP-Fplus, 50 T, IVD-CE	Thrombophilia Genetic Disease Screen with 677 C>T and 1298 A>C MTHFR mutations	More Information
SS007B2	Elucigene Ashplex 2, 50 T, IVD-CE	Ashkenazi Genetic Disease Screen, ARMS based, 50 Tests	More Information
AS008B2	Elucigene Ashplex 1, 50 T, IVD-CE	Ashkenazi Genetic Disease Screen, ARMS based, 50 Tests	More Information
AA002B2	Elucigene AAT, 50 T, IVD-CE	AAT deficiency Genetic Disease Screen, Gel Analysis Technique, 50 Tests	More Information
TH003B2	Elucigene TRP, 50 T, IVD-CE	Thrombophilia Genetic Disease Screen, Gel Analysis Technique, 50 Tests	More Information
THF03B2	Elucigene TRP-F, 50 T, IVD-CE	Thrombophilia Genetic Disease Screen, QF-PCR Analysis Technique, 50 Tests	More Information