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
FMF07B2 Elucigene FMF, 50 T, IVD-CE Familial Mediterranean Fever Disease Screen, ARMS Based, 50 Tests More Information
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