What is genetic research?

Name: Genetic thrombophilia profile
Brand: სინევო
SKU: PL260401
Price: 570 GEL
Availability: InStock
Rating: 5 (1 reviews)

Genetic research is research that identifies gene mutations or their consequences (e.g., changes in metabolites)

* 7770

info@synevo.ge

The site is temporarily down due to maintenance. Sorry for the inconvenience.

Laboratory tests

Quality & Accuracy

Experience

The latest technologies

Speed &
Credibility

Genetic thrombophilia profile

Synevo editorial team

Known as: Hereditary thrombophlilia profile

SKU: PL260401

Original price was: ₾1,250.00.Current price is: ₾570.00.

Research material: blood

Response time (working day): 14

The test is done on an empty stomach: no

Home call service: Yes

Country: EU

Laboratories❯

General Information

Genetic thrombophilia

Sampling for research will be done:

In the regions:on Thursday
In Tbilisi: Thursday and/or Friday until 12:00

Samples will be sent on Friday! For this, it is necessary to bring the sample to the central laboratoryUntil 12:00 on Friday!

What is genetic thrombophilia?

Thrombophilia is a condition in which the probability of blood clots is increased. This condition is called hypercoagulation. Thrombophilia may be congenital or acquired.

What are the causes of genetic thrombophilia?

Acquired thrombophilia is more common than congenital, and its cause may be: diseases, some medications, and others. The most common cause of acquired thrombophilia is antiphospholipid syndrome
Genetic (hereditary) thrombophilia is the result of a mutation that an individual receives from one of their parents. The issue of genetic thrombophilia becomes relevant in case of history of terminated pregnancies, presence of thrombosis before the age of 40.

The diagnostic profile for genetic thrombophilia includes the following tests:

• Prothrombin gene mutation (factor II) G20210A
• Factor V Leiden mutation G1691A
• PAI-1 gene (polymorphism 675 4G/5G)
• MTHFR gene (C677T, A1298C mutations)
• Factor XIII gene mutation (G102T)

When should we take the test?

Genetic testing for thrombophilia should be performed Only in high-risk groups Or when the outcome actually determines treatment and prevention.

Genetic thrombophilia testing is recommended in the following cases:

Venous thromboembolism (VTE), associated with pregnancy, the postpartum period, or hormonal contraceptives
Thrombosis in unusual locations – For example, in the veins of the brain or abdomen
A strong family history – Especially if family members have high-risk thrombophilias (antithrombin, protein C, or protein S deficiency)
Women planning hormone therapy or pregnancy and have a family history of severe thrombophilia

Reference values

material Material: Venous blood (EDTA 3 tubes)

Hypercoagulable state: Genetic changes cause overactivity of the blood clotting system
Deficiency of natural anticoagulants: Antithrombin, protein C, and protein S are natural anticoagulants. Their deficiency is associated with the development of thrombophilia.
Fibrinolysis disorder: After a blood clot forms, the process of clot dissolution slows down, which increases the likelihood of the clot persisting and spreading.

What are the risk factors for thrombosis?

Excess weight

Pregnancy

Tobacco consumption

Atherosclerosis

Tumor

diabetes

Immovable lifestyle

Postoperative condition

Oral contraception

Hormone replacement therapy

Family history of hypercoagulation

old age

Terminated pregnancies

At least one episode of thrombosis before the age of 40

Other tests

Testing process


Purchase a test	Submission of material


Results Online	Consult a doctor

Resources

https://my.clevelandclinic.org/health/diseases/21797-thrombophilia

News and promotions

Chronic inflammation and mental health | What you need to know

Learn more »

Human Papillomavirus (HPV) Screening Campaign – Until August 31

Learn more »

Summer promotion for patients aged 65+

Learn more »

Gestational Diabetes | What you need to know

Learn more »

Laboratories

Select a location

Synevo

4.9

Based on 273 reviews

review us on

This medical information is not intended to be a universal treatment guide for all patients. The treatment process, including the type, volume, and frequency of diagnostic tests and therapeutic procedures, is determined by the physician individually — based on an assessment of the patient's condition and relevant medical indications. The decision is made in consultation with the patient. Before purchasing a test, please read the instructions for its preparation.