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Medical information Clinical review pending

Genetic Testing

RPS28 Gene Diamond Blackfan Anemia Type 15 with Mandibulofacial Dysostosis Genetic Test

Genetic test using Next Generation Sequencing (NGS) to detect mutations in the RPS28 gene, associated with Diamond Blackfan Anemia Type 15 and Mandibulofacial Dysostosis. Helps in diagnosing this rare blood disorder.

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 patient preparation is required. Please provide a detailed clinical history and family history, including a pedigree chart if available. Confirm specific requirements 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 RPS28 Gene Diamond Blackfan Anemia Type 15 with Mandibulofacial Dysostosis 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 Diamond Blackfan Anemia (DBA)
  • ✓Presence of physical features associated with Mandibulofacial Dysostosis
  • ✓Family history of DBA or related genetic conditions
  • ✓Unexplained severe anemia in infancy or childhood
  • ✓Genetic counseling for individuals with potential risk factors
02

In plain language

What this test helps you understand

This test helps confirm or rule out a diagnosis of Diamond Blackfan Anemia Type 15 associated with RPS28 gene mutations. It can aid in understanding the genetic basis of the condition, guiding treatment decisions, and providing information for genetic counseling within families.
This genetic test identifies mutations in the RPS28 gene, which are linked to Diamond Blackfan Anemia (DBA) Type 15 and Mandibulofacial Dysostosis. DBA is a rare inherited condition affecting red blood cell production, often presenting with anemia and physical differences. Understanding the specific genetic cause can guide diagnosis and management. This test uses advanced Next Generation Sequencing (NGS) technology for accurate detection of relevant mutations in the RPS28 gene. Early diagnosis allows for appropriate medical care and potential interventions.
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. Please provide a detailed clinical history and family history, including a pedigree chart if available. Confirm specific requirements with the laboratory before booking.
SampleBlood sample (EDTA tube), extracted DNA, or one drop of blood on an FTA card.
MethodologyNext Generation Sequencing (NGS) is used to analyze the RPS28 gene for specific mutations.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test specifically analyzes the RPS28 gene. It may not detect mutations in other genes associated with Diamond Blackfan Anemia or similar conditions. Results should be interpreted in conjunction with 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

DBA is a rare, inherited bone marrow failure syndrome characterized by a failure to produce enough red blood cells, leading to anemia. It often presents in infancy or early childhood.
Mandibulofacial Dysostosis refers to a group of genetic disorders affecting the development of facial bones and tissues.
Individuals with symptoms suggestive of DBA, such as severe anemia, fatigue, or specific physical features, especially with a family history of related conditions, should consider this test.
Results indicate the presence or absence of specific mutations in the RPS28 gene. A genetic counselor or physician will explain the findings and their implications.
Yes, genetic counseling is highly recommended before and after testing to understand the test's implications, interpret results, and discuss family risks.
A blood sample, extracted DNA, or a single drop of blood on an FTA card can be used. Please confirm the preferred sample type with the laboratory.
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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