When is it necessary to conduct genetic studies for infertility?

Name: Rodinia - Thrombophilia and NAIT panel (additional panel when performing a couple infertility panel**) (22 options)
Brand: სინევო
SKU: GEN-ROD005MG
Price: 1570 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

* 7770

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Rodinia – Thrombophilia and NAIT panel (additional panel when conducting a couple infertility panel**) (22 options)

Synevo editorial team

Known as: Rodinia-THROMBOPHILIA AND NAIT PANEL ADD-ON PANEL to the couples panel 22 variants

SKU: GEN-ROD005MG

₾1,570.00

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

Laboratories❯

General Information

**You will receive the study at the indicated price, Rodinia – Female and Male Infertility Panel in Couples (55 Genes / 40 Genes) After conducting, as an additional study.

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 interpreting research resultsLaboratory""Synevo"We offer MEDICOVER GeneticsGeneticist's freeConsultation

What is the Rodinia Thrombophilia and NAIT panel?

Rodinia – Thrombophilia and NAIT panel (additional panel when conducting a couple infertility panel**) (22 options)

The Thrombophilia and Neonatal Alloimmune Thrombocytopenia (NAIT) panel identifies genetic variations that increase the risk of conditions such as:

Early or late termination of pregnancy
Thrombosis
Neonatal alloimmune thrombocytopenia

(Neonatal alloimmune thrombocytopenia (NAIT) is a rare but serious condition in newborns caused by the mother's immune system attacking the fetus' platelets during pregnancy.)

The panel ensures the identification of individuals at risk before life-threatening conditions develop, allowing for management of the condition and reduction of complications.

Rodinia – Thrombophilia and NAIT Panel (standalone panel) can be used both individually and as an additional test in male and female infertility panel studies.

When should we take the test?

Who is the test for?

Couples and individuals with more than one prematurely terminated pregnancy
Newborns with thrombocytopenia
Individuals with an early onset episode of thrombocytopenia or a clear family history.
Individuals with recurrent episodes of thrombosis
Newborns with unexplained thrombosis

Study sample:Cheek swab

Possible interpretation of the results

Rodinia Thrombophilia and NAIT Panel There is additional research in the diagnostics of infertility. The final interpretation of research results should always be made in the clinical and genetic context.

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

How many genes are being studied?

The panel will examine 17 genetic variants in 22 genes.

genes

NM_000130.4(F5):c.1601G>A (p.Arg534Gln). NM_000130.4(F5):c.3980A>G (p.His1327Arg). NM_000129.3(F13A1):c.103G>T (p.Val35Leu). NM_000212.2(ITGB3):c.176T>C (p.Leu59Pro). NM_000173.7(GP1BA):c.482C>T (p.Thr161Met). NM_000419.5(ITGA2B):c.2621T>G (p.Ile874Ser). NM_000212.2(ITGB3):c.506G>A (p.Arg169Gln). NM_002203.4(ITGA2):c.1600G>A (p.Glu534Lys). NM_000212.2(ITGB3):c.1544G>A (p.Arg515Gln). NM_000602.5(SERPINE1):c.-820G[(4_5)]. NM_005957.5(MTHFR):c.665C>T (p.Ala222Val). NM_005957.4(MTHFR):c.1286A>C (p.Glu429Ala). NM_000789.3(ACE):c.2306-117_2306-116insAF118569.1:g.14094_14382. NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln). NM_000041.2(APOE):c.526C>T (p.Arg176Cys). NM_000041.4(APOE):c.388T>C (p.Cys130Arg). NM_000254.2(MTR):c.2756A>G (p.Asp919Gly). NM_002454.3(MTRR):c.66A>G (p.Ile22Met). NM_000029.4(AGT):c.803T>C (p.Met268Thr). NM_031850.3(AGTR1):c.*86A>C. NM_000852.4(GSTP1):c.313A>G (p.Ile105Val). NM_000506.5(F2):c.*97G>A.

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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.