Medical information Clinical review pending

Genetic Testing

Aldob Gene Fructose Intolerance Genetic Test

Genetic test to identify mutations in the ALDOB gene associated with fructose intolerance, a metabolic disorder. Uses Next-Generation Sequencing (NGS) technology.

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), extracted DNA, or one drop of blood on an FTA card.
Results: Approximately 3 to 4 weeks. Confirm with the laboratory before booking.
Preparation: No specific fasting is required. Confirm with the laboratory before booking. A pre-test consultation and genetic counseling session are recommended to discuss the test and provide a clinical history, including a family pedigree chart if possible.

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 Aldob Gene Fructose Intolerance 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.

✓Symptoms suggestive of fructose intolerance (e.g., abdominal pain, vomiting, hypoglycemia after fructose intake).
✓Family history of fructose intolerance or related metabolic disorders.
✓Individuals with unexplained metabolic issues.
✓Confirmation of suspected fructose intolerance.
✓Genetic counseling for family planning.

In plain language

What this test helps you understand

This test helps confirm or rule out a diagnosis of fructose intolerance caused by mutations in the ALDOB gene. It aids in identifying individuals at risk, allowing for appropriate dietary management and prevention of complications associated with fructose consumption. Results can also inform family planning decisions.

The Aldob Gene Fructose Intolerance NGS Genetic DNA Test is a diagnostic tool used to identify mutations in the ALDOB gene. This gene provides instructions for making the enzyme aldolase B, which is essential for breaking down fructose. A deficiency or malfunction of this enzyme leads to fructose intolerance, a metabolic disorder that can cause serious health issues if not managed properly. Early diagnosis through genetic testing is crucial for effective management and lifestyle adjustments. This test utilizes Next-Generation Sequencing (NGS) technology for accurate detection of mutations.

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 specific fasting is required. Confirm with the laboratory before booking. A pre-test consultation and genetic counseling session are recommended to discuss the test and provide a clinical history, including a family pedigree chart if possible.

SampleBlood sample (EDTA tube), extracted DNA, or one drop of blood on an FTA card.

MethodologyNext-Generation Sequencing (NGS) is used to analyze the ALDOB gene for mutations.

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

This test specifically analyzes the ALDOB gene. It may not detect all possible genetic causes of fructose intolerance symptoms. Results should be interpreted in conjunction with clinical findings and family history. Confirm with the laboratory before booking.

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

Fructose intolerance is a metabolic disorder where the body cannot properly break down fructose, a type of sugar found in fruits, honey, and some processed foods. This can lead to various symptoms after consuming fructose.

Genetic testing can identify specific mutations in the ALDOB gene that cause fructose intolerance, confirming the diagnosis and helping individuals manage their diet effectively to avoid symptoms and complications.

Individuals experiencing symptoms like abdominal pain or hypoglycemia after eating fructose, or those with a family history of fructose intolerance, should consider this test.

The test involves analyzing a sample of your blood or DNA to look for mutations in the ALDOB gene. A consultation and genetic counseling are recommended before testing.

Results will indicate the presence or absence of specific mutations in the ALDOB gene. A genetic counselor can help interpret the results and discuss their implications for you and your family.

Yes, genetic counseling is highly recommended before and after the test to understand the purpose, potential results, and implications of the 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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