thrombophilia-screening

Thrombophilia Screening

Stop the clot to secure a healthy future!

Thrombophilia is a common genetic blood disorder affecting blood coagulation, thereby increasing the risks of Thrombosis and pulmonary embolism. Hereditary Thrombophilia can be inherited in an autosomal dominant manner i.e., one non-affected copy is enough to cause the disease. Such individuals are more likely to develop clots than healthy individuals. Heterozygous individuals have around 50% of normal plasma Antithrombin levels and are usually symptomatic.Homozygous deficiency is incompatible with life.

Test Price: ₹5500.00

thrombophilia-screening
Coverage
Coverage

Thrombophilia mutation profiling is a cost effective and sensitive test which screens the most common 14 gene mutations responsible for Thrombophilia.

LEARN MORE

Parameters covered are - Factor V (G1691A) Leiden, Factor II Prothrombin (G20210A), MTHFR (C677T), MTHFR (A1298C), MTRR (A66G),MTR (A2756G),PAI SERPINE (-675 5G/4G), FGB (G-455A), AGT 1 (C521T), AGT 2 (C4072T), FVII (G1238A), FXIII (G103T), ITGA2 (C807T), ITGB3 (T176C)

MyFitBabyPlus

Stepping into Motherhood ?
MyBabyFitPlus
Benefits

FREE Sample Collection

PAN India Logistics

Accurate Reporting

Fast TAT

Stringent QC

You Might also Like

clinical-exome-sequencing
Clinical Exome Sequencing

Whole Genome coverage without compromise on delivering excellence in specificity, sensitivity and resolution. learn more >

₹35000.00 ADD TO CART
thalscreen-panel
THALSCREEN Panel
Don't Delay, Screen Today.

Don't Delay, Screen Today. learn more >

₹5000.00 ADD TO CART
ibrandox