Initial Consultation
A detailed review of the family tree (minimum three generations) and reproductive history.
Genetic Counseling
Advanced Genomic Insights at Gynatal Timișoara
Genetic counseling at Gynatal Clinic (Timișoara) is a specialized medical evaluation led by our experts to identify risks of hereditary diseases and optimize IVF success. Depending of each couple’s histioty, The process integrates Karyotyping, Carrier Screening, and non-invasive embryo testing (ni-PGT-A)A standard consultation costs 300 RON, providing a scientific roadmap to assess reproductive genetic risks and support informed repreductive decisions.
What is Genetic Counseling in Fertility Care?
Genetic counseling is an in-depth analysis of the personal and family medical history of both partners. It aims to identify genetic alterations that could affect reproductive potential, fetal development, or long-term health. At Gynatal, we don't just provide tests; we offer a comprehensive interpretation that links genetic findings directly to your IVF protocol to maximize the chance of a successful, full-term pregnancy.
Who Should Seek Genetic Counseling?
While beneficial for any couple planning a family, specialized counseling is strongly recommended for:
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Recurrent Miscarriages: Two or more consecutive losses, which may be caused by balanced chromosomal translocations in the parents.
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Failed IVF Cycles: Repeated implantation failure despite transferring "good-quality embryos.
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Advanced Maternal Age (>35-37): To manage the increased risk of numerical chromosomal abnormalities (aneuploidies), such as Down syndrome.
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Family History: Known hereditary conditions like cystic fibrosis, spinal muscular atrophy (SMA), thalassemia, or hemophilia.
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Severe Male Factor: Severe oligozoospermia or azoospermia, which can be linked to Y-chromosome microdeletions.
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Previous pregnancy with genetic disorder
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Consanguinity: couples who are biologically related may benefit from additional genetic risk assessement
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Known genetic variant: one partner is known to carry a pathogenic genetic variant
The Gynatal Genetic Roadmap
As part of the international FutureLife network, we apply a "Scientific Gold Standard" diagnostic pathway:
Carrier Screening
Testing both partners for recessive mutations. If both carry the same mutation, there is a 25% risk of the child being affected.
Parental Karyotyping
Analyzing the structure and number of parental chromosomes to detect "silent" abnormalities.
Advanced Lab Analysis
Utilizing Next Generation Sequencing (NGS) for maximum precision in results.
IVF with PGT
When clinically indicated, we recommend IVF with embryo testing (PGT-M for monogenic diseases or PGT-A for chromosomal health).
Non-Invasive Testing (ni-PGT-A)
This method analyzes the DNA released by the embryo into the culture medium.
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Non-invasive: No embryo biopsy is required, as analysis is performer usig cell-free DNA from the culture medium
- Additional Embryo information: may provide complementary information to support embryo selection in selected patients
Frequently Asked Questions (FAQ)
Can we have a healthy child if we carry a genetic disease?
Yes. Through PGT-M technology, we can identify embryos that have not inherited the specific family condition and select only healthy ones for transfer.
How long do results take?
Due to the complexity of DNA sequencing, results are typically available within 3 to 4 weeks.