When is it necessary to conduct genetic studies for infertility?

Name: Rodinia - Female and Male Infertility Panel in Couples (55 Genes / 40 Genes)
Brand: სინევო
SKU: GEN-ROD004MG
Price: 2950 GEL
Availability: InStock
Rating: 5 (1 reviews)

Genetic studies of infertility are necessary in cases of a long history of infertility, Spontaneous abortions with abortion pills , Genetic diseases In the presence of a family history , or when artificial insemination is planned ( IVF procedure

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Rodinia – Female and Male Infertility Panel in Couples (55 Genes / 40 Genes)

Synevo editorial team

Known as: Rodinia – Both partners (male & female infertility panel) (55 genes/40 genes)

SKU: GEN-ROD004MG

₾2,950.00

Research material: buccal mucosa smear

Response time (working day): 25

The test is done on an empty stomach: no

Home call service: Yes

Country: EU

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General Information

The cost of the study for 2 people is 5900 GEL.

Sampling for research will be done:

In the regions: Thursday
In Tbilisi: Thursday and/or Friday (in the first half of the day)

Samples will be sent on Friday afternoon! For this, the sample must be sent to the central laboratory by Friday 12:00.

For the interpretation of the research results, the Synevo laboratory offers a free consultation with a geneticist from MEDICOVER Genetics.

What is Rodinia?

Rodinia is a study that provides screening for genetic mutations associated with infertility.

Infertility is a major pathology of the reproductive system in which conception and maintenance of pregnancy are difficult or impossible.

Worldwide, 6 in every 1 couples experience infertility. 35% of infertility cases are due to male infertility, and 45% to female infertility. The remaining cases are the result of a combination of both causes.

Infertility has many different causes, including genetic ones. Laboratory studies, ultrasound imaging, and sperm analysis reveal 65% of infertility cases. Genetic causes of infertility are observed in 10-15% of men and women.

Genetic tests for infertility investigate these causes, allowing for informed decision-making and optimal clinical management of the condition.

Study sample:Cheek swab

Genes (male)

ANOS1, AR, AURKC, CATSPER1, CFTR, CHD7, DAZL, DDX25, DUSP6, FEZF1, FGF8, FGF17, FGFR1, FLRT3, FMR1, FSHB, FSHR, GNRH1, GNRHR, HESX1, HS6ST1, IL17RD, KISS1, KISS1R, LHB, LHCGR, NR5A1, NSMF, PRM1. PROK2, PROKR2, SEMA3A, SPRY4, SRD5A1, SRY, TAC3, TACR3, USP26, USP9Y, WDR11

Genes (female)

AIRE, ANOS1, BMP15, CAPN10, CHD7, CYP11A1, CYP17A1, CYP19A1, DENND1A, DUSP6, EIF2B2, EIF2B3, FEZF1, FGF8, FGF17, FGFR1, FIGLA, FLRT3, FMR1, FOXL2, FSHB, FSHR, GALT, GDF9, GNAS, GNRH1, GNRHR. HESX1, HS6ST1, IL17RD, INS, INSR, IRS1, IRS2, KISS1, KISS1R, LHB, LHCGR, NOBOX, NR5A1, NSMF, POF1B, POLG, PROK2, PROKR2, PSMC3IP, SEMA3A, SPRY4, STAG3, TAC3, TACR3, THADA, WDR11, WT1, ZP1

When should we take the test?

When is the survey conducted?

Rodinia – Genetic research for infertility can help:

Identify genetic causes of infertility
Provide accurate forecasting
To determine the optimal treatment plan for the couple or individual
Resolve the need for intervention in a timely manner

Possible interpretation of the results

Male infertility panel (40 genes) Includes:

X and Y chromosome research
Detection of Y chromosome microdeletions
The manifestation of hypogonadotropic hypogonadism (Kalman syndrome)

Female infertility panel (55 genes) Includes:

The panel tests for 55 genes as well as X chromosome aneuploidies.

Reference values

Important information

The buccal mucosa sample should be collected immediately after opening the package.
60 minutes before sample collection, the patient is prohibited from: smoking, taking food and liquids (except water), brushing teeth and chewing gum
Please follow the instructions for specimen labelling, collection and transport carefully.
Check that all patient identification data is correct and compliant before specimen packaging and shipping

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Testing process


Purchase a test	Submission of material


Results Online	Consult a doctor

Resources

http://medicovergenetics.com

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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.