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₾1,790.00
Adventia – basic panel (1 person)
The Adventia Baseline Panel examines 22 genes whose mutations are associated with high frequency and severity of disease.
The research is conducted with Target Capture Enrichment technology, using a new generation sequencing method.
The Adventia Basic Panel tests for the following diseases:
Samples will be sent on Friday afternoon! For this, the sample must be sent to the central laboratory by Friday 12:00.
The taken sample is sent and the research is conducted in the laboratory of MEDICOVER Genetics in a laboratory with international accreditation.
Test results are available within 20 working days of sampling. The answer will be sent to the E-mail address of the doctor and the patient. at the post office. It is also possible to receive on-site laboratory center.
If necessary, Synevo Laboratory offers a consultation with a geneticist.
The sample collection and transport kit is intended for the collection, transport and storage of material required for genetic research, according to the specified procedure.
Sample collection Device: Two (2) buccal swab collection devices
Packaging materials: One (1) biosecurity bag to seal the specimen
Sample collection instructions
For assistance or to order additional kits, please call +(995)32 2 800 111 or email us at info@synevo.ge. Additional information is available online at Synevo.ge
Adventia is a new generation genetic test that determines whether a phenotypically healthy person is a carrier of a genetic disease.
Adventia allows diagnostics of autosomal and X-linked recessive disease. Carriers of recessive diseases have one healthy gene and one gene with a mutation.
The information obtained from the Adventia genetic test helps us make reproductive decisions and minimizes the number of people who can pass on genetic diseases to their offspring.
Any person can be a carrier of this or that mutation (mutation – permanent change in the nucleotide sequence of DNA). Some mutations have no effect on human health, while others cause genetic diseases.
When a person is a carrier of a specific gene mutation, but this mutation is not strong enough to cause the disease to manifest in the individual - this is a recessive gene carrier for the disease. If both parents carry the same gene mutation and their child inherits the mutation from both of them, the child will be affected.
Carrying a recessive gene mutation is asymptomatic, therefore the individual has no information about the risk of passing this mutation on to the offspring.
A number of recessive disease genes may be transmitted from generation to generation without symptoms.
Early knowledge of carrier status and the risk of passing on genetic disorders to children makes it possible to:
According to the recommendation of international organizations, information about pregnancy screening should be available to all pregnant women; Simultaneous screening for multiple conditions is recommended.
Other tests




Testing process
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Purchase a test |
Submission of material |
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Results Online |
Consult a doctor |
https://medicover-genetics.com/our-genetic-tests/reproductive-health/carrier-screening/