Medical information Clinical review pending

Genetic Testing

FOXRED1 Gene Leigh Syndrome Genetic Test

Genetic test using Next-Generation Sequencing (NGS) to identify mutations in the FOXRED1 gene associated with Leigh syndrome, a neurological disorder. Helps in early diagnosis and management.

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) or Saliva sample (collection kit provided). Confirm specific requirements with the laboratory before booking.
Results: Confirm with the laboratory before booking.
Preparation: No special preparation is typically required for a blood or saliva sample. Confirm with the laboratory before booking.

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 FOXRED1 Gene Leigh Syndrome 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.

Talk to a claims advisor

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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Mobile number *

+254

Insurer or scheme

Policy / member number (optional)

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.

✓Infants or children presenting with symptoms suggestive of Leigh syndrome (e.g., developmental delays, muscle weakness, seizures, respiratory difficulties).
✓Individuals with a family history of Leigh syndrome or related neurological disorders.
✓Patients where clinical suspicion for a mitochondrial disorder is high.
✓Genetic counseling for families with a history of Leigh syndrome.
✓Confirmation of diagnosis in suspected cases.

In plain language

What this test helps you understand

Identifies mutations in the FOXRED1 gene, a known cause of Leigh syndrome. Aids in the diagnosis of this severe neurological disorder, particularly in infants and young children. Provides information for prognosis, genetic counseling, and family planning.

The FOXRED1 Gene Leigh Syndrome NGS Genetic DNA Test is an advanced diagnostic tool used to identify genetic factors linked to Leigh syndrome. This is a severe neurological disorder that primarily affects infants and young children, often leading to progressive neurological decline. The test utilizes Next-Generation Sequencing (NGS) technology to analyze the FOXRED1 gene. This gene plays a vital role in mitochondrial function and energy production within the brain. Early diagnosis through genetic testing is crucial as it can significantly influence treatment decisions and management strategies, providing families with important information regarding their child's health. This test specifically looks for mutations within the FOXRED1 gene, which are known causes of Leigh syndrome. Identifying these genetic changes allows healthcare providers to assess the risk of developing the disorder and develop appropriate management plans.

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 a blood or saliva sample. Confirm with the laboratory before booking.

SampleBlood sample (EDTA tube) or Saliva sample (collection kit provided). Confirm specific requirements with the laboratory before booking.

MethodologyNext-Generation Sequencing (NGS) of the FOXRED1 gene.

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

This test only analyzes the FOXRED1 gene. Leigh syndrome can be caused by mutations in other genes. A negative result does not completely rule out Leigh syndrome or other genetic conditions. Interpretation requires clinical correlation.

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

Leigh syndrome is a severe neurological disorder that typically affects infants and young children, causing progressive loss of mental and movement abilities.

Mutations in the FOXRED1 gene are a known cause of Leigh syndrome. This test identifies these specific genetic changes.

Individuals with symptoms suggestive of Leigh syndrome, a family history of the condition, or those advised by a healthcare professional or genetic counselor should consider this test.

Results are interpreted by a medical geneticist or qualified healthcare provider, often in conjunction with genetic counseling, to understand the implications for diagnosis and management.

A negative result means no mutations were found in the FOXRED1 gene. It does not rule out Leigh syndrome, as other genes can cause it. Further testing or clinical evaluation may be needed.

Confirm with the laboratory before booking.

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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