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Genetic Testing

NBAS Gene Infantile Liver Failure Syndrome Type 2 Genetic Test

This genetic test identifies mutations in the NBAS gene associated with Infantile Liver Failure Syndrome Type 2, using Next Generation Sequencing (NGS) technology. It aids in diagnosing genetic causes of severe liver dysfunction in infants.

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
A blood sample (usually collected in an EDTA tube) from the infant. Confirm specific requirements with the laboratory before booking.
Results
Approximately 3 to 4 weeks. Confirm with the laboratory before booking.
Preparation
No special preparation is typically required for the infant. 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 NBAS Gene Infantile Liver Failure Syndrome Type 2 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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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

01

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 with symptoms suggestive of liver failure (e.g., severe jaundice, failure to thrive, hypoglycemia, coagulopathy).
  • ✓Family history of infantile liver failure or related genetic disorders.
  • ✓Confirmation of suspected NBAS gene-related liver disease.
  • ✓Genetic counseling for families with affected children.
  • ✓Prenatal diagnosis in high-risk pregnancies (requires specific consultation).
02

In plain language

What this test helps you understand

This test helps identify specific genetic mutations in the NBAS gene linked to Infantile Liver Failure Syndrome Type 2. Early diagnosis can guide treatment strategies and management plans for affected infants.
The NBAS Gene Infantile Liver Failure Syndrome Type 2 NGS Genetic DNA Test is an advanced diagnostic procedure designed to identify mutations in the NBAS gene that can lead to severe liver dysfunction in infants. This test plays a vital role in the early diagnosis and management of liver failure syndromes, enabling timely interventions that can significantly improve health outcomes.

This genetic test utilizes Next Generation Sequencing (NGS) technology to detect alterations in the NBAS gene. By analyzing the genetic material from the patient, the test helps ascertain whether a genetic mutation is present that may contribute to infantile liver failure.

Parents or guardians should consider this test for infants exhibiting symptoms such as severe jaundice, failure to thrive, hypoglycemia, or coagulopathy. Additionally, families with a history of liver disorders or genetic conditions affecting liver function may also benefit from this testing.

Benefits of taking this test include early diagnosis of genetic liver disorders, informed decision-making regarding treatment options, guidance for family planning and genetic counseling, and access to specialized care tailored to the specific genetic condition.

Results from the NBAS Gene test will be provided after a turnaround time of approximately 3 to 4 weeks. A genetic counselor will assist in interpreting the results, discussing their implications, and guiding families on the next steps based on the findings.
03

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 →
04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

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.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

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 the infant. Confirm with the laboratory before booking.
SampleA blood sample (usually collected in an EDTA tube) from the infant. Confirm specific requirements with the laboratory before booking.
MethodologyNext Generation Sequencing (NGS) of the NBAS gene.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test specifically analyzes the NBAS gene. It will not detect mutations in other genes that can cause liver failure. The test may not identify all possible mutations within the NBAS gene. Results should be interpreted in the context of clinical findings and family history. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

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.
07

Questions people ask

Frequently asked questions

This is a rare genetic disorder caused by mutations in the NBAS gene, leading to severe liver problems in infants shortly after birth.
Early diagnosis allows for appropriate medical management, helps families understand the condition, and informs decisions about future family planning.
A blood sample is typically required from the infant. Please confirm specific collection details with the laboratory.
A genetic counselor will help explain the test results, discuss their meaning, and provide guidance on next steps.
Insurance coverage varies. Please check with your insurance provider regarding coverage for genetic testing.
08

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.

Explore partnerships
09

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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