MIR17HG Gene Feingold syndrome type 2 NGS Genetic Test
Short Name: Feingold Syndrome Type 2 NGS Test
Also known as: Feingold Syndrome Type 2, MIR17HG Gene Feingold Syndrome Type 2
MIR17HG Gene Feingold syndrome type 2 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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
To detect mutations in the MIR17HG gene for the diagnosis of Feingold Syndrome Type 2, aiding in clinical management and genetic counseling.
- Test Code
- 4931
- 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
- NGS Technology
Sample Collection
Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Feingold Syndrome Type 2.
Method: Blood Draw
Laboratory Analysis
Blood sample collected via venipuncture.
Report Delivery
Sample sent to laboratory for NGS analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To detect mutations in the MIR17HG gene for the diagnosis of Feingold Syndrome Type 2, aiding in clinical management and genetic counseling.
How to Prepare
- Ensure proper sample labeling
- Use sterile equipment
- Store sample at ambient room temperature
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing is crucial for confirming Feingold Syndrome Type 2, enabling early intervention and family counseling."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Insufficient sample volume
- Improper labeling
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis of Feingold Syndrome Type 2. Genetic counseling recommended.
Negative for pathogenic variant
No mutations detected in MIR17HG gene. Consider other genetic or clinical evaluations.
Variant of uncertain significance
Further testing or family studies may be needed for clarification.
If symptoms such as microcephaly, hypertelorism, or developmental delays are present, or if there is a family history of Feingold Syndrome Type 2.
Limitations
- ⚠May not detect all genetic variants
- ⚠Results require clinical correlation
Risks & Considerations
- ●Minor bruising at blood draw site
- ●Rare risk of infection
Interfering Factors
- ●Poor sample quality
- ●Contamination during collection
Frequently Asked Questions
What is Feingold Syndrome Type 2?
What are the symptoms of Feingold Syndrome Type 2?
How is Feingold Syndrome Type 2 diagnosed?
What is the cost of the MIR17HG Gene Feingold Syndrome Type 2 NGS Genetic Test?
Is home sample collection available for this test?
How long does it take to get the test results?
What sample is required for the test?
Is fasting required before the test?
Who should consider this test?
What does a positive test result mean?
Can this test be done for prenatal diagnosis?
Is genetic counseling recommended before testing?
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₹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.
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✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
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