NEXMIF Gene Mental retardation, X-linked, nonsyndromic NGS Genetic Test
Short Name: NEXMIF Gene Mental Retardation NGS Test
Also known as: X-linked Nonsyndromic Mental Retardation, NEXMIF-related Intellectual Disability
NEXMIF Gene Mental retardation, X-linked, nonsyndromic 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 SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To diagnose mutations in the NEXMIF gene responsible for X-linked nonsyndromic mental retardation, aiding in clinical management and genetic counseling.
- Test Code
- 1702
- 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
No specific preparation required. Provide clinical history and pedigree chart for genetic counseling.
Method: Venipuncture or FTA card collection
Laboratory Analysis
Blood sample drawn via venipuncture or one drop on FTA card.
Report Delivery
Sample sent to laboratory for NGS analysis. Reports delivered in 3-4 weeks.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose mutations in the NEXMIF gene responsible for X-linked nonsyndromic mental retardation, aiding in clinical management and genetic counseling.
How to Prepare
- Use sterile equipment for blood collection
- Label samples correctly
- Store FTA card at ambient temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"This test is essential for diagnosing X-linked mental retardation caused by NEXMIF gene mutations, aiding in genetic counseling and family planning."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed sample
- Incorrect labeling
- Insufficient sample
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis of NEXMIF-related mental retardation. Genetic counseling recommended.
Negative for pathogenic variant
No variants detected; clinical correlation and additional tests may be needed.
Variant of uncertain significance
Further family studies and clinical evaluation required.
If symptoms of intellectual disability, developmental delays, or seizures are present, consult a neurologist or geneticist for evaluation.
Limitations
- ⚠Test may not detect all variants due to technical limitations
- ⚠Results require clinical correlation
- ⚠Does not rule out other genetic causes
Risks & Considerations
- ●Minimal risk from blood draw: bruising, infection at site.
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Insufficient sample volume
Compare With Similar Tests
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| Comparison | NEXMIF Gene Mental retardation, X-linked, nonsyndromic NGS Genetic Test |
Frequently Asked Questions
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