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AAAS Full Gene Sequence Analysis (Allogrove Syndrome) Test

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AAAS Full Gene Sequence Analysis (Allogrove Syndrome) Test

AAAS Full Gene Sequence Analysis (Allogrove Syndrome) Test test available at DNA Labs India for ₹30,000. Uses Sanger Sequencing on Peripheral blood, Amniotic Fluid, Chorionic Villi, Cord Blood samples. Results in 2-3 weeks. Free home collection in 300+ cities across India.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Allogrove Syndrome by detecting mutations in the AAAS gene through full gene sequence analysis.

Test Code
2933
Price
₹30,000
Sample Type
Peripheral blood, Amniotic Fluid, Chorionic Villi, Cord Blood
Result Time
2-3 weeks
Fasting Required
No
Method
Sanger Sequencing
Step 1

Sample Collection

Ensure a doctor's prescription is available. No specific preparation required unless advised by physician.

Method: Venipuncture or as per sample type

Step 2

Laboratory Analysis

Sample collected via venipuncture or appropriate method based on sample type.

Step 3

Report Delivery

Apply pressure to the collection site to prevent bleeding. Store samples as instructed.

Timeline: 2-3 weeks

Patient Instructions

1
Before the Test:Obtain doctor's prescription. No fasting required.
2
During the Test:Sample collection procedure as per standard protocols.
3
After the Test:Wait for report delivery in 2-3 weeks. Follow up with physician.

About This Test

Who Should Get This Test

To diagnose Allogrove Syndrome by detecting mutations in the AAAS gene through full gene sequence analysis.

How to Prepare

  • Use sterile containers as specified
  • Label samples correctly
  • Transport with cool pack if needed

Doctor's Notes

Reviewed by — MBBS, MD (General Medicine) · Reg. No. 8052

"Genetic testing for Allogrove Syndrome is essential for early diagnosis and management. This test provides accurate results to guide clinical decisions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypePeripheral blood, Amniotic Fluid, Chorionic Villi, Cord Blood
ContainerSterile container, Sterile Normal Saline Container, EDTA Vacutainer (2ml)
Collection MethodVenipuncture or as per sample type

Sample Stability

Peripheral blood: 24-48 hours at room temperature
Amniotic fluid: 24 hours refrigerated
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient volume
  • Improper labeling

Understanding Your Results

Results indicate the presence or absence of mutations in the AAAS gene associated with Allogrove Syndrome.
Positive result: Pathogenic mutation detected, confirming diagnosis
Negative result: No mutation detected, but clinical correlation is advised
Variant of uncertain significance: Further testing or consultation recommended
⚠️ When to Consult a Doctor:

Consult a geneticist or specialist if symptoms persist or if test results are positive for management guidance.

Risks & Considerations

  • Minor bruising at collection site
  • Rare infection risk

Frequently Asked Questions

What is Allogrove Syndrome?
Allogrove Syndrome is a rare genetic disorder caused by mutations in the AAAS gene, affecting multiple body systems including immune, endocrine, and nervous systems.
What does the AAAS Full Gene Sequence Analysis test for?
This test examines the entire AAAS gene for mutations to confirm a diagnosis of Allogrove Syndrome.
How is the test performed?
The test uses Sanger Sequencing to analyze DNA from samples like peripheral blood, amniotic fluid, chorionic villi, or cord blood.
What samples are required?
Peripheral blood, amniotic fluid, chorionic villi, or cord blood collected in sterile containers or EDTA vacutainers.
Is fasting required for this test?
No, fasting is not required for the AAAS Full Gene Sequence Analysis.
How long does it take to get results?
Results are typically available within 2-3 weeks after sample collection.
Is the test covered by insurance?
This test is generally not covered by insurance and is paid out of pocket.
What is the cost of the test?
The cost is INR 30000, with free home sample collection available across India.
Are there any risks associated with the test?
Risks are minimal, such as minor bruising from blood draw, but serious complications are rare.
How accurate is the test?
The AAAS Full Gene Sequence Analysis is highly accurate for detecting mutations in the AAAS gene.
Can the test be done during pregnancy?
Yes, using amniotic fluid or chorionic villi samples, but a doctor's prescription is required.
What should I do if the test is positive?
Consult a geneticist or specialist for further evaluation, management, and genetic counseling.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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