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Test Name: | Thrombophilia Mutation Detection |
Compliance: | LDT |
Test Description: | Thrombophilia or hypercoagulability is an inherited or acquired susceptibility to thrombosis (blood clots) due to abnormal coagulability of the clotting system. The association of prothrombin (F2) gene and Factor V Leiden mutations with an increased risk for venous thrombosis has been well documented. MTHFR mutations dramatically increase risk for venous thrombosis when present with other genetic thrombophilic factors. |
Methodology: | PCR-Sanger sequencing detection of hotspot mutations on F2, F5 and MTHFR genes |
Gene Name: | F2, F5, MTHFR |
Protein Name: | |
Specimen Requirements: | EDTA Blood (5mL) |
Storage Condition: | Ambient Temperature / 4℃ (if overnight is needed) |
Turn Around Time: | 5 working days from day of specimen received |
OMIM: | |
Genetic Home Reference: | |
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Personal health information or related information released to HKMPDC relating to the services requested may be subjected to re-disclosure by HKMPDC to health care providers, such as doctors, nurses, and others involved in the delivery of the services.
We may also disclose medical information about you to authorised public health or government officials for public health activities as required by law and accreditation body.
Copyright © 2013 香港分子病理檢驗中心 Hong Kong Molecular Pathology Diagnostic Centre Limited (HKMPDC). All Rights Reserved.
Information Updated 1 July, 2023.
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