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DNA Labs India

Microcephaly Gene Panel Test

DNA Labs India | ISO 9001:2015 Certified

Microcephaly Gene Panel Test

Also known as: Microcephaly Genetic Panel, Microcephaly DNA Test

Microcephaly Gene Panel Test test available at DNA Labs India for ₹36,000. Uses Next-Generation Sequencing (NGS) on Amniotic fluid/ Chorionic villi/ Peripheral blood samples. Results in 4-6 weeks. Free home collection in 300+ cities across India.

Genetic TestInfants and children🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SHAILAJA RAGHUNATH MURDESHWAR

Dr SHAILAJA RAGHUNATH MURDESHWAR

Consultant Physician · Reg: 8052

Last reviewed: September 7, 2026

Overview

To identify genetic mutations associated with microcephaly for accurate diagnosis, treatment planning, and genetic counseling.

Test Code
3094
Price
₹36,000
Sample Type
Amniotic fluid/ Chorionic villi/ Peripheral blood
Result Time
4-6 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Microcephaly Gene Panel can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Method: Venipuncture for blood, amniocentesis for amniotic fluid, chorionic villus sampling for chorionic villi

Step 2

Laboratory Analysis

Sample collected by a trained phlebotomist or healthcare professional using sterile techniques.

Step 3

Report Delivery

Sample is labeled, stored appropriately, and transported to the laboratory for analysis.

Timeline: 4-6 weeks

Patient Instructions

1
Before the Test:Consult a doctor for prescription and pre-test counseling.
2
During the Test:Sample collection procedure as per instructions.
3
After the Test:Wait for results and follow up with healthcare provider for interpretation.

About This Test

Who Should Get This Test

To identify genetic mutations associated with microcephaly for accurate diagnosis, treatment planning, and genetic counseling.

How to Prepare

  • Use sterile container for sample collection
  • Maintain cool pack during transport for blood samples
  • Follow specific instructions for amniotic fluid or chorionic villi collection

Doctor's Notes

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

"This test is crucial for early diagnosis and management of microcephaly in infants, aiding in genetic counseling and treatment planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid/ Chorionic villi/ Peripheral blood
Sample Volume3 ml for blood
ContainerSterile container/ Sterile Normal Saline Container/ EDTA Vacutainer(3 ml)
Collection MethodVenipuncture for blood, amniocentesis for amniotic fluid, chorionic villus sampling for chorionic villi

Sample Stability

Blood sample stable for 48 hours at 2-8°C
Amniotic fluid and chorionic villi should be processed immediately
Sample Rejection Criteria:
  • Hemolyzed or insufficient sample volume
  • Improperly labeled or contaminated samples
  • Sample not stored at recommended temperature

Understanding Your Results

Results indicate the presence or absence of genetic mutations associated with microcephaly, aiding in diagnosis and management.
Positive: Pathogenic variant detected, indicating genetic cause for microcephaly
Negative: No pathogenic variants detected, but clinical correlation is advised
Variant of Uncertain Significance (VUS): Further testing or clinical evaluation may be needed
⚠️ When to Consult a Doctor:

If symptoms of microcephaly are present, for genetic counseling, or to discuss test results and management options.

Limitations

  • ⚠May not detect all genetic causes of microcephaly
  • ⚠Variants of uncertain significance may be identified
  • ⚠Does not rule out non-genetic causes

Risks & Considerations

  • ●Minimal risk from blood draw, such as bruising or infection
  • ●Risk of inconclusive or uncertain results
  • ●Psychological impact of genetic findings

Interfering Factors

  • ●Sample contamination
  • ●Improper storage or transport
  • ●Hemolyzed blood sample

Compare With Similar Tests

TestMicrocephaly Gene PanelMicrocephaly Imaging (CT/MRI)Chromosomal Analysis
ComparisonMicrocephaly Gene Panel

Frequently Asked Questions

What is the Microcephaly Gene Panel test?
It is a comprehensive genetic test that analyzes over 90 genes associated with microcephaly to identify specific mutations causing the condition.
Who should take this test?
Infants or children with symptoms like small head size, developmental delays, or seizures, and families with a history of microcephaly.
How is the test performed?
The test uses Next-Generation Sequencing (NGS) on samples such as blood, amniotic fluid, or chorionic villi.
What is the cost of the test?
The cost is INR 36,000, inclusive of home sample collection in many cities across India.
How long does it take to get results?
Results are typically available within 4-6 weeks after sample collection.
Is home sample collection available?
Yes, free home sample collection is available for online bookings in numerous cities across India.
Do I need a doctor's prescription?
Yes, a doctor's prescription is required, except for surgery, pregnancy, or travel abroad cases.
What samples are required?
Samples can be amniotic fluid, chorionic villi, or peripheral blood, collected in sterile containers.
What are the risks of the test?
Risks are minimal, such as bruising from blood draw, but there may be psychological impacts from genetic findings.
How accurate is the test?
The test uses advanced NGS technology for high accuracy, but it may not detect all genetic causes or may identify variants of uncertain significance.
Can the test detect all causes of microcephaly?
No, it focuses on genetic causes and may not detect non-genetic factors or all genetic mutations.
What should I do after receiving the results?
Consult a healthcare professional or genetic counselor to interpret results and discuss management options.
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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For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

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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