FLNA Gene Heterotopia, periventricular, X-linked dominant NGS Genetic Test
Short Name: FLNA Gene Heterotopia Test
Also known as: Periventricular Heterotopia, X-linked, FLNA-related Periventricular Nodular Heterotopia
FLNA Gene Heterotopia, periventricular, X-linked dominant 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 diagnose FLNA Gene Heterotopia Periventricular X-Linked Dominant by detecting mutations in the FLNA gene using NGS technology, enabling early management and genetic counseling.
- Test Code
- 4554
- 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 special preparation needed. Provide clinical history and family pedigree chart.
Method: Venipuncture for blood sample
Laboratory Analysis
Blood sample will be drawn from a vein in the arm.
Report Delivery
Apply pressure to the puncture site to stop bleeding.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose FLNA Gene Heterotopia Periventricular X-Linked Dominant by detecting mutations in the FLNA gene using NGS technology, enabling early management and genetic counseling.
How to Prepare
- Ensure sample is collected in a sterile container
- Label sample correctly with patient details
- Transport sample at ambient temperature
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"As an obstetrician-gynecologist, I recommend genetic testing for females with a family history of neurological disorders to enable early intervention and family planning."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or insufficient sample
- Incorrect labeling
- Contaminated sample
Understanding Your Results
Pathogenic variant detected
Confirms FLNA Gene Heterotopia diagnosis
No pathogenic variant detected
Unlikely to have the disorder, but clinical correlation is needed
Variant of uncertain significance
Requires genetic counseling and possible family studies
If symptoms such as seizures or developmental delays persist, or if there is a family history of the disorder.
Limitations
- ⚠May not detect all types of mutations
- ⚠Requires interpretation by a geneticist
- ⚠Not a diagnostic tool for all neurological disorders
Risks & Considerations
- ●Minimal risks from blood draw, such as bruising or infection
- ●Psychological impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Technical errors in sequencing
Compare With Similar Tests
| Test | FLNA Gene Heterotopia, periventricular, X-linked dominant NGS Genetic Test | Whole Exome Sequencing | Chromosomal Microarray | Sanger Sequencing | MRI Brain |
|---|---|---|---|---|---|
| Comparison | FLNA Gene Heterotopia, periventricular, X-linked dominant NGS Genetic Test |
Frequently Asked Questions
What is FLNA Gene Heterotopia?
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Why choose DNA Labs India for this test?
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