Thrombocheck Hereditary
A panel that specifically tests for hereditary platelet disorders, helping to diagnose genetic causes of thrombocytopenia, platelet dysfunction, or clotting disorders.
Thrombocheck Hereditary Package in Vadodara Overview
What is Thrombocheck Hereditary test?
The Thrombocheck Hereditary test is a specialized genetic and biochemical panel that helps identify inherited (genetic) causes of thrombophilia, a condition where blood has an increased tendency to clot. The Thrombocheck Hereditary panel focuses solely on inherited thrombophilia, helping distinguish genetic causes from acquired clotting risks. Early identification enables targeted prevention
Parameter Covered: PROTIEN C, FREE PROTIEN S, ANTITHROMBIN ACTIVITY, HOMOCYSTEINE,
FACTOR V
Why consider Thrombocheck Hereditary test?
Thrombocheck Hereditary test can be considered
- To identify inherited clotting disorders in individuals with a personal or family history of thrombosis.
- To guide preventive or therapeutic anticoagulant treatment
- To assess risk before major surgery, pregnancy, or hormonal therapy (e.g., oral contraceptives).
Who should get tested for Thrombocheck Hereditary test ?
Thrombocheck Hereditary test can be recommended for
- Individuals with unexplained or recurrent blood clots.
- Those with a strong family history of venous thromboembolism.
- Women with recurrent miscarriages or complications during pregnancy.
- People who developed clots at a young age or in unusual sites (like cerebral or abdominal veins).
More Information
OTHER NAMES: Hereditary Thrombophilia Panel, Genetic Thrombophilia Profile, Inherited Thrombosis Risk Evaluation
Thrombophilia is a medical condition in which the blood has an increased tendency to form abnormal clots (thrombi) in veins or arteries. These clots can partially or completely block normal blood flow, leading to serious health problems such as deep vein thrombosis (DVT), pulmonary embolism (PE), stroke, or recurrent pregnancy loss. Thrombophilia can be inherited (genetic) or acquired (developed later in life).
Types of Thrombophilia
- Inherited (Genetic) Thrombophilia: Caused by genetic mutations passed from parents to children.
- Acquired Thrombophilia: Develops later due to medical conditions or external factors.
No special preparations needed
- Protein C Activity
- Antithrombin
- Homocysteine
- Factor V Leiden Mutation
- Free Protein S
Test code
7980
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Edta Whole Blood | Lavender Vacutainer | 3 ML |
| Plasma Citrate | Blue Vacutainer | 3 ML |
| Plasma Edta | Lavender Vacutainer | 1 ML |
| Serum | Yellow Vacutainer | 1 ML |
Specimen stability information
Edta Whole Blood, Plasma Citrate
Specimen rejection criteria
Test run frequency
'
Turn around time
Same Day
Performing locations
Department
- Advanced Molecular Diagnostics R&d
- Coagulation
- Bio Chemistry
CPT and Loinc codes
Package price
₹14500
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₹14500