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Reliable clinical communication
How results are explained and what happens next matter as much as the result itself.
Omega Genetics SMA Carrier Screening
Learn Your SMA Carrier
Risk Early
With Omega Genetics expertise, we offer a clear, reassuring and guided SMA carrier-assessment pathway for preconception and prenatal planning.
✓ Omega Genetics specialist assessment✓ Preconception and prenatal support✓ Nationwide sample coordination
Carrier frequency
1 / 50
SMA carrier status is seen at a notable frequency in Türkiye.
Prenatal assessment
10+
Further assessment options can be planned early in pregnancy for carrier couples.
When both partners are carriers
Risk distribution for each pregnancy
25%
Affected child
50%
Carrier child
25%
Non-carrier child
These probabilities should be interpreted within genetic counselling.
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Molecular-analysis focus
Genetic analysis is planned with the clinical context in mind.
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Action at the right time
Timing before and during pregnancy directly affects available decisions.
Why does carrier assessment matter?
SMA risk is often invisible until carrier status is identified
Preconception screening is therefore both a test and a decision-support process.
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Carrier frequency is significant in Türkiye
Approximately one in 50 people is an SMA carrier, so risk becomes visible through systematic screening.
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Risk rises when both partners are carriers
If both parents are carriers, each pregnancy has a 25% affected-child and 50% carrier-child probability.
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Early knowledge supports planning
Assessment before or during pregnancy helps families manage subsequent decisions consciously.
Who is it for?
Testing needs should be assessed as part of the couple’s shared planning
SMA assessment is especially relevant for couples planning pregnancy, people with a family history and those with a known carrier result.
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Couples planning pregnancy
Knowing carrier status before conception enables more controlled risk assessment.
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People with a family history
A family history of SMA or unexplained infant loss makes genetic screening more important.
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People seeking pre-marital genetic assessment
Carrier screening can provide informed decision support before marriage.
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People with an identified carrier result
If one partner is a carrier, the other should be assessed and prenatal planning considered if needed.
When is it performed?
Correct timing determines the benefit of testing
SMA assessment serves different purposes before pregnancy and during the prenatal period for carrier couples.
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Preconception carrier screening
This is the ideal time. A simple blood sample supports risk assessment and planning before pregnancy.
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Prenatal assessment during pregnancy
For carrier couples, chorionic villus sampling or amniocentesis may be considered with a physician.
Testing process
We simplify the process and reduce uncertainty
Every step, from first contact to result guidance, is planned to support clinical decisions.
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Initial discussion and clinical information
We call you, review family history and clarify the most suitable pathway.
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Sample coordination
Our Ankara-based laboratory infrastructure supports sample acceptance and guidance throughout Türkiye.
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Genetic analysis
The sample is examined with appropriate molecular methods and interpreted for carrier or prenatal risk.
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Result communication and guidance
Findings are explained clearly and further counselling is planned where needed.
The Omega Genetics approach
The goal is not only to produce a result, but to put it in the right context
SMA testing involves carrier status, prenatal options and subsequent clinical decisions. We treat content, communication and guidance with equal care.
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Omega Genetics expertise
Genetic testing requires accurate interpretation and guidance as well as technical analysis.
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Nationwide service coverage
Sample and communication processes are coordinated across Türkiye, not only Ankara.
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Prenatal-compatible approach
We provide a clear framework for prenatal diagnostic options when risk is identified.
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Clear result communication
We translate complex genetic terminology into everyday language.
⌂ Ankara central laboratory
Omega Genetics laboratory
Ankara-based laboratory with nationwide service coverage
Our central laboratory, where molecular genetic analyses are performed, is located on Piri Reis Caddesi in Beytepe, Ankara. Sample acceptance and communication are coordinated from anywhere in Türkiye, with courier and routing organised by our team.
Ankara
Central laboratory location
TR
Nationwide sample network
3
Supported languages
Home sample collection
Home sample collection is organised by Omega Çare, our specialist home healthcare team.
Frequently asked questions
What people most often ask about SMA carrier screening
Your question may not be listed. Contact our team for information relevant to you.
SMA carrier screening results are generally ready within 7–10 business days. Transport time to the laboratory may affect this period. Results are announced by email and SMS.
Quick contact
Get information from our specialist team
Let us call you about sample coordination, timing, carrier-couple risk and prenatal assessment.
Contact form
Let us call you and clarify the process together
Our team will contact you about testing time, sample flow and the assessment steps suitable for you.
☎ +90 507 743 86 88