MYCN Gene Feingold syndrome NGS Genetic Test
Short Name: Feingold Syndrome NGS Test
MYCN Gene Feingold syndrome NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of this test is to identify mutations in the MYCN gene and other genes associated with Feingold syndrome using Next Generation Sequencing technology. It aids in the definitive diagnosis of the disorder, guiding clinical management and genetic counseling.
- Test Code
- 2738
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 weeks
- Fasting Required
- No
- Method
- Next Generation Sequencing (NGS)
Sample Collection
Provide clinical history and undergo genetic counseling.
Method: Venipuncture or finger prick
Laboratory Analysis
Blood sample will be collected via venipuncture or finger prick.
Report Delivery
Apply pressure to the puncture site to prevent bruising.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to identify mutations in the MYCN gene and other genes associated with Feingold syndrome using Next Generation Sequencing technology. It aids in the definitive diagnosis of the disorder, guiding clinical management and genetic counseling.
How to Prepare
- Fast for 8-12 hours if required, but for genetic tests, fasting is not typically needed.
- Bring identification and prescription.
- Inform about any medications.
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing with NGS technology provides a comprehensive analysis for accurate diagnosis of Feingold syndrome, enabling early intervention and management."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or insufficient sample
- Incorrect labeling
- Contaminated sample
Understanding Your Results
If symptoms of Feingold syndrome are present or if there is a family history, consult a geneticist or pediatrician for evaluation and testing.
Limitations
- ⚠May not detect all genetic variants
- ⚠Results require interpretation by a geneticist
- ⚠Does not rule out other genetic conditions
Risks & Considerations
- ●Minimal risk from blood draw
- ●Potential psychological impact of results
Frequently Asked Questions
What is Feingold syndrome?
What causes Feingold syndrome?
What are the symptoms of Feingold syndrome?
How is Feingold syndrome diagnosed?
What is the MYCN gene?
What is NGS genetic testing?
How much does the MYCN Gene Feingold Syndrome NGS Genetic Test cost?
What sample is required for the test?
How long does it take to get results?
Is home sample collection available?
What should I do if the test is positive?
Can this test be used for prenatal diagnosis?
Related Tests
Amino Acids Qualitative Two Dimensional Urine Test
₹1,439Succinylacetone Urine Test
₹5,000RXFP2 Gene Cryptorchidism NGS Genetic Test
₹20,000EFNB1 Gene Craniofrontonasal syndrome NGS Genetic Test
₹20,000MNX1 Gene Currarino syndrome NGS Genetic Test
₹20,000FGFR1 Gene Craniosynostosis, FGFR1 related NGS Genetic Test
₹20,000Reference 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.
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.
Book Your Test
Enter your details and we'll connect you within 15 minutes.