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Genetic Disorders
Genetic Disorders


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:
Phone: +852.2986.1213
Fax:+852.2527.7028
E-mail:contact@hk-mpdc.com
27/F., Strand 50, No.50 Bonham Strand, Sheung Wan, Hong Kong
Opening Hours
Mondays to Fridays: 09:00-18:00
Saturdays: 09:00-16:00
Sundays and Public Holidays: Closed

For specimen pickup arrangements, please phone +852.2986.1213


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