Genetic Testing
ATR Gene Seckel Syndrome Type 1 Genetic Test
Genetic test using Next-Generation Sequencing (NGS) to detect mutations in the ATR gene associated with Seckel syndrome. Helps identify genetic predispositions and guide medical decisions.
General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.
Review status: No completed medical review is recorded for this page.
At a glance
Plan your test
- Sample
- Blood sample (EDTA tube) or Saliva sample (collection kit provided). Confirm with the laboratory before booking.
- Results
- 3 to 4 weeks. Confirm with the laboratory before booking.
- Preparation
- No special preparation is required for a blood draw. If using a saliva kit, follow the instructions provided carefully. Confirm with the laboratory before booking.
Payment: M-Pesa and card options can be confirmed during booking.
Insurance & government schemes
Is this test covered for you?
We help you verify whether the ATR Gene Seckel Syndrome Type 1 Genetic Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.
Providers & schemes we can help you check
Government & public schemes
Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.
Private insurers & employer schemes
Names shown for identification only — listing does not imply partnership or guarantee of coverage.
Have these ready when we check
- Insurer or scheme name & policy / member number
- A clinician's request / prescription for the test
- Pre-authorisation letter, if your plan requires one
Free coverage check
Ask us to verify your cover
Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.
Start with fit
Is this the right test for you?
The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.
- ✓Individuals with clinical features suggestive of Seckel syndrome (e.g., severe growth retardation, distinctive facial features, developmental delays).
- ✓Family members of individuals diagnosed with Seckel syndrome.
- ✓Prenatal diagnosis in families with a known history of ATR gene mutations.
- ✓Confirmation of diagnosis in cases with atypical presentation.
- ✓Genetic counseling for families with a history of related genetic disorders.
In plain language
What this test helps you understand
This test specifically detects mutations in the ATR gene, which are known to cause Seckel syndrome. By analyzing the genetic code, healthcare providers can identify whether an individual carries the genetic markers associated with this condition.
Individuals or families with a history of Seckel syndrome or related dysmorphological features should consider this test. Symptoms may include severe growth retardation, distinctive facial features, neurological issues, and developmental delays. Additionally, those with a family history of genetic disorders or those experiencing unexplained health issues may also benefit from this test.
Taking this test can help identify genetic predispositions for Seckel syndrome, guide families in understanding their health risks, enable informed decision-making regarding family planning and medical management, and offer peace of mind through genetic insights.
Results will typically be available within 3 to 4 weeks. A positive result indicates the presence of ATR gene mutations, while a negative result suggests that no such mutations were detected. It’s essential to discuss the results with a genetic counselor or healthcare provider to understand their implications fully.
Medical review status
Clinical review pending
A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.
Meet the DNA Labs Kenya medical team →A simple process
What happens next?
You do not have to navigate the test alone. We help you move from question to next step.
Speak with us
We check the test and answer your questions before collection.
Give your sample
Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.
Understand your report
A counselor helps you understand the result and the next steps.
Choose your collection
Home collection or a lab visit
We will explain the sample, preparation, and next steps before anything is collected.
Home collection
Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.
Lab or hub visit
Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.
Ask about locations →Read your report
What common result terms mean
Questions people ask
Frequently asked questions
Collaboration
Open for partnership with hospitals, clinics, doctors & researchers
Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.
Hospitals & clinics
Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.
Doctors & specialists
LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.
Research institutions
Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.
Students & academic projects
Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.
Trust & transparency
Sources, standards & how this page is maintained
Standards & references
- ACMG/AMP technical standards for sequence variant interpretation
- ClinGen curation and gene–disease validity frameworks where applicable
- LOINC-coded reporting for interoperable results
- ISO 9001:2015 quality management; ISO 15189 accreditation in progress
Page provenance
- Last updated: September 27, 2026
- Medical review: not yet completed
- Written for patients & clinicians in Kenya; reviewed periodically against current guidance
Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.
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