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Medical information Clinical review pending

Genetic Testing

Steroid Panel for Premature Adrenarche Test

A specialized test to evaluate hormone levels in children showing early signs of sexual maturation, helping to identify potential adrenal gland disorders.

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
2 mL serum collected in a red top tube (no additive). Avoid SST gel barrier tubes.
Results
Typically 2 days for samples collected on Monday or Thursday. Confirm with the laboratory before booking.
Preparation
Sample collection should occur between 8-10 am or 4-6 pm. Please specify the time and date on the specimen container and test request form.
Test priceKSh 9,000

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 Steroid Panel for Premature Adrenarche 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.

  • ✓Early development of secondary sexual characteristics in children
  • ✓Rapid growth spurts in children
  • ✓Suspected premature adrenarche
  • ✓Family history of adrenal disorders
  • ✓Evaluation of adrenal hormone levels
02

In plain language

What this test helps you understand

This test helps identify hormonal imbalances related to adrenal gland function in children presenting with signs of premature adrenarche.
The Steroid Panel for Premature Adrenarche Test is a diagnostic tool used to assess hormone levels in children who may be experiencing early signs of sexual development. This test is important for identifying disorders related to the adrenal glands, which can affect a child's health if not managed properly.

This comprehensive panel measures several key hormones related to adrenal function, including Androstenedione, DHEA (Dehydroepiandrosterone), DHEAS (Dehydroepiandrosterone sulfate), 17-Hydroxyprogesterone, Total Testosterone (Ultrasensitive), and Estradiol (Ultrasensitive).

This test is recommended for children exhibiting symptoms such as early development of secondary sexual characteristics, rapid growth spurts, or other signs of premature adrenarche. Children with a family history of adrenal disorders may also benefit from this test.

Taking this test can help in the early detection of hormonal imbalances and guide appropriate medical intervention. Results will be provided, detailing the levels of each hormone tested. It is essential to consult with a qualified healthcare provider, such as an endocrinologist, to interpret these results accurately and discuss any necessary follow-up actions.
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 →
PreparationSample collection should occur between 8-10 am or 4-6 pm. Please specify the time and date on the specimen container and test request form.
Sample2 mL serum collected in a red top tube (no additive). Avoid SST gel barrier tubes.
MethodologyConfirm with the laboratory before booking.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
Results must be interpreted in the context of the patient's clinical presentation and other relevant investigations. 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

Premature adrenarche is the early onset of adrenal androgen production, leading to signs of puberty like pubic hair, body odor, and sometimes acne, before the typical age.
This test helps identify hormonal imbalances that may be causing premature adrenarche and can rule out other underlying conditions affecting the adrenal glands.
A qualified healthcare provider, often an endocrinologist, will interpret the results in the context of your child's overall health and symptoms.
The sample is collected via a blood draw, specifically 2 mL of serum in a red top tube.
Yes, the sample should be collected at a specific time (8-10 am or 4-6 pm). Please follow the instructions provided by 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.

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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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