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Genetic Testing

ANKRD11 Gene KBG Syndrome Genetic Test

Genetic test to identify mutations in the ANKRD11 gene, associated with KBG syndrome. Helps diagnose the condition, characterized by developmental delays and distinct facial features.

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 a single drop of blood on an FTA card.
Results
Approximately 3 to 4 weeks. Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required. A clinical history of the patient is necessary prior to testing. Genetic counseling is recommended.
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 ANKRD11 Gene KBG 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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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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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.

  • ✓Suspected KBG syndrome based on clinical features.
  • ✓Developmental delays or intellectual disability.
  • ✓Distinctive facial features suggestive of KBG syndrome.
  • ✓Family history of KBG syndrome.
  • ✓Need for genetic confirmation for diagnosis.
  • ✓Genetic counseling and family planning.
02

In plain language

What this test helps you understand

This test helps confirm a diagnosis of KBG syndrome by identifying mutations in the ANKRD11 gene. It can aid in understanding the specific genetic cause of the condition in an individual, which may inform management strategies and prognosis. Results can also be used for genetic counseling and family planning.
The ANKRD11 Gene KBG Syndrome NGS Genetic DNA Test is a specialized genetic analysis designed to detect mutations within the ANKRD11 gene. These mutations are known to cause KBG syndrome, a genetic disorder often associated with developmental delays, intellectual disabilities, and specific physical characteristics. Understanding the genetic basis of KBG syndrome is important for managing the condition and for family planning purposes. This test uses Next Generation Sequencing (NGS) technology to analyze the patient's genetic material for alterations in the ANKRD11 gene. A clinical history of the patient is required before testing, and genetic counseling is recommended, especially for families with a history of KBG syndrome or related disorders.
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 specific patient preparation is required. A clinical history of the patient is necessary prior to testing. Genetic counseling is recommended.
SampleBlood sample (EDTA tube), extracted DNA, or a single drop of blood on an FTA card.
MethodologyNext Generation Sequencing (NGS) is used to detect mutations in the ANKRD11 gene.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test specifically analyzes the ANKRD11 gene. It will not detect mutations in other genes that might cause similar symptoms. A negative result does not completely rule out KBG syndrome, as some mutations may not be detected by this method. 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

KBG syndrome is a genetic disorder characterized by developmental delays, intellectual disability, and distinctive facial features. It is caused by mutations in the ANKRD11 gene.
Individuals showing symptoms of KBG syndrome, such as developmental delays or specific facial features, and families with a history of the condition should consider this test.
A blood sample, extracted DNA, or a single drop of blood on an FTA card is required for the test.
The turnaround time is typically 3 to 4 weeks. Confirm with the laboratory before booking.
A positive result indicates that a mutation in the ANKRD11 gene associated with KBG syndrome has been identified.
Yes, genetic counseling is recommended before and after testing to discuss the implications of the results and family planning.
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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