Genetic tests for the comprehensive examination of male/female infertility
Working Time
- Mon-Thu 08:00 – 20:00
Friday 07:00 – 22:00
Saturday 08:00 – 18:00
Contact Info
- Phone: 1-800-267-0000
1-800-267-0001
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Genetic tests for the comprehensive examination of female infertility
Female Fertility Tests
Genetic centre iVF Riga offers a new service for patients – an opportunity to make a comprehensive check of women’s health, which will help to answer the question why the long-awaited pregnancy does not occur. Received results will help to avoid possible risks of losing pregnancy in the future and to develop the further treatment plan for a successful result.
Indications for a comprehensive examination for women with the following anamnesis:
- Abortus habitualis (two or more missed ab.)
- Stopped pregnancy for unclear reasons in the second or third trimester
- Failed implantation (negative result after the previous cycle of IVF treatment)
- Early pregnancy loss (spontaneous abortion)
- Premature ovarian failure
The comprehensive examination includes:
- Molecular testing for thrombophilia (F5, F2 and MTHFR gene variants)
- PAI determination (Plasminogen activator inhibitor) for in-depth examination of predisposition to congenital thrombophilia
- Testing for the Fragile X chromosome syndrome to clarify the etiology of premature ovarian failure
- Determination of the karyotype (number of chromosomes)
The results can be obtained after 4 weeks.
Genetic tests for the comprehensive examination of male infertility
Male Fertility Tests
Genetic centre iVF Riga offers a new service for patients – an opportunity to make a comprehensive check of men’s health, which will help to answer the question why the long-awaited pregnancy does not occur in his female partner. Received results will help to develop the further examination and treatment plan to achieve a successful result.
Indications for a comprehensive examination for men:
If a man wants to know if he could become a father:
- In cases of azoospermia or oligozoospermia (absence or very low concentration of spermatozoa in the ejaculate)
- In his female partner does not occur pregnancy for a year or more of regular sexual life without the use of any contraceptive
- There are repeated pregnancy losses on the early term (two or more spontaneous abortions) in his female partner anamnesis
- Failed implantation in the female partner (negative result after the previous cycle of IVF treatment)
The comprehensive examination includes:
- Molecular testing for determination of AZF region microdeletions of Y-chromosome
- Determination of the karyotype (number of chromosomes)
- Determination of the most common CFTR gene mutations that cause cystic fibrosis (mucoviscidosis)
- Determination of hereditary hemochromatosis – genetically caused disorder, which is characterized by excessive accumulation of iron in the body’s tissues and organs, including testicular tissues. Excessive iron accumulation can cause a gradual cessation of spermatogenesis.
The results can be obtained after 4 weeks.
Sign up: +371 67111117 or genetikascentrs@ivfriga.eu