Medical information Clinical review pending

Genetic Testing

ASL Gene Argininosuccinic Aciduria Genetic Test

Genetic test using Next Generation Sequencing (NGS) to detect mutations in the ASL gene associated with argininosuccinic aciduria, a rare metabolic disorder. A Genetic Counseling session is recommended before testing.

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: Confirm with the laboratory before booking.
Preparation: A clinical history of the patient is required. A Genetic Counseling session is recommended to draw a pedigree chart of family members affected with argininosuccinic aciduria.

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 ASL Gene Argininosuccinic Aciduria 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.

✓Symptoms suggestive of a metabolic disorder (e.g., developmental delays, seizures, neurological issues).
✓Family history of argininosuccinic aciduria or related metabolic disorders.
✓Abnormal results from preliminary metabolic screening tests.
✓Carrier screening in families with a known history of the disorder.

In plain language

What this test helps you understand

This test helps diagnose argininosuccinic aciduria, a rare inherited metabolic disorder. Identifying the specific genetic mutation can guide management strategies and inform family members about potential risks.

The ASL Gene Argininosuccinic Aciduria NGS Genetic DNA Test is a specialized diagnostic tool used to identify mutations in the ASL gene, which are responsible for argininosuccinic aciduria, a rare metabolic disorder. This test employs Next Generation Sequencing (NGS) technology, allowing for a comprehensive analysis of the genetic material. Early diagnosis through this test is crucial as it can lead to timely interventions and management of the disorder, significantly improving the quality of life for affected individuals. This genetic test detects specific mutations in the ASL gene that may lead to argininosuccinic aciduria. By analyzing the DNA, healthcare providers can determine if a patient has inherited the disorder and assess the potential risks for family members. Results from the ASL Gene Argininosuccinic Aciduria NGS Genetic DNA Test will be provided in a clear and comprehensive report. A healthcare professional will guide you through the findings, explaining whether mutations were detected and what they mean for your health and that of your family. It is essential to have a follow-up consultation to discuss the implications of the results.

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 →

PreparationA clinical history of the patient is required. A Genetic Counseling session is recommended to draw a pedigree chart of family members affected with argininosuccinic aciduria.

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

MethodologyNext Generation Sequencing (NGS) of the ASL gene.

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

This test primarily analyzes the ASL gene. It may not detect mutations in other genes that could cause similar symptoms. 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

Argininosuccinic aciduria is a rare inherited metabolic disorder affecting the body's ability to process protein. It is caused by mutations in the ASL gene.

Genetic counseling helps patients and families understand the test, its implications, potential risks, and the meaning of the results. It is particularly important for inherited conditions.

The report will indicate if any mutations in the ASL gene were detected. A healthcare professional will explain the findings and their significance for diagnosis and management.

This test focuses on mutations within the ASL gene. While comprehensive, it may not detect all possible genetic changes. Discuss specific concerns with your doctor.

Insurance coverage varies. Please check with your insurance provider regarding coverage for genetic testing.

A blood sample, extracted DNA, or a single drop of blood on an FTA card can be used. Our team can advise on the best collection method.

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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