Medical information Clinical review pending

Genetic Testing

CAMTA1 Gene Cerebellar Ataxia Nonprogressive with Mental Retardation Genetic Test

Genetic test to identify mutations in the CAMTA1 gene associated with nonprogressive cerebellar ataxia and intellectual disabilities, using Next-Generation Sequencing (NGS).

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.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample: Blood sample (EDTA tube). Confirm specific requirements with the laboratory before booking.
Results: Confirm with the laboratory before booking.
Preparation: No special preparation is typically required for this blood test. However, confirm with the laboratory for any specific instructions.

Test priceKSh 40,000

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 CAMTA1 Gene Cerebellar Ataxia Nonprogressive with Mental Retardation 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.

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Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

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.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

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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 unexplained balance and coordination problems.
✓Individuals with intellectual disabilities or developmental delays.
✓Family history of cerebellar ataxia or related neurological disorders.
✓Symptoms suggestive of nonprogressive cerebellar ataxia.
✓Confirmation of diagnosis when clinical suspicion is high.

In plain language

What this test helps you understand

This test helps identify specific genetic mutations in the CAMTA1 gene linked to nonprogressive cerebellar ataxia and intellectual disabilities. It aids in confirming a diagnosis, understanding the underlying cause of symptoms, and informing management strategies. Results can also be used for genetic counseling regarding family risks and potential inheritance patterns.

The CAMTA1 Gene Cerebellar Ataxia Nonprogressive with Mental Retardation NGS Genetic DNA Test is a specialized genetic analysis designed to detect mutations within the CAMTA1 gene. These mutations are linked to specific neurological conditions characterized by nonprogressive cerebellar ataxia (affecting balance and coordination) and intellectual disabilities. This test utilizes advanced Next-Generation Sequencing (NGS) technology for a detailed examination of the gene. Understanding the genetic basis of these conditions can aid in diagnosis, management, and genetic counseling. Early detection can help guide appropriate care and support strategies for affected individuals and their families.

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.

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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 →

PreparationNo special preparation is typically required for this blood test. However, confirm with the laboratory for any specific instructions.

SampleBlood sample (EDTA tube). Confirm specific requirements with the laboratory before booking.

MethodologyNext-Generation Sequencing (NGS) of the CAMTA1 gene.

PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.

This test specifically analyzes the CAMTA1 gene. It does not detect mutations in other genes that may cause similar symptoms. A negative result does not completely rule out a genetic cause for the condition. Interpretation of results requires clinical correlation and may benefit from genetic counseling.

Read your report

What common result terms mean

TermPlain-language meaning

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.

NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.

VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.

Questions people ask

Frequently asked questions

The CAMTA1 gene provides instructions for making a protein important for normal brain development and function. Mutations in this gene are associated with nonprogressive cerebellar ataxia and intellectual disability.

Symptoms often include problems with balance and coordination (ataxia), intellectual disability, and sometimes speech difficulties. The condition is typically nonprogressive, meaning symptoms do not worsen over time.

This test is recommended for individuals showing symptoms like balance issues, intellectual disability, or developmental delays, especially if there is a family history of similar conditions. Consult your doctor.

Results indicate whether specific mutations in the CAMTA1 gene were found. A genetic counselor or your doctor can help interpret the results in the context of your clinical picture and family history.

Yes, genetic counseling is highly recommended to discuss the test results, understand their implications for health and family planning, and explore available resources.

Turnaround time varies. Please confirm the current estimated turnaround time with the laboratory before booking your test.

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.

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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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