FLVCR2 Gene Hydranencephaly, Fowler type NGS Genetic Test
Also known as: Fowler type hydranencephaly, FLVCR2-related hydranencephaly
FLVCR2 Gene Hydranencephaly, Fowler type 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 SHAILAJA RAGHUNATH MURDESHWAR
Consultant Physician · Reg: 8052
Last reviewed: September 7, 2026
Overview
To identify mutations in the FLVCR2 gene that cause hydranencephaly, Fowler type, aiding in diagnosis, genetic counseling, and family planning.
- Test Code
- 5784
- 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 of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected with the disorder.
Method: Venipuncture or FTA card collection
Laboratory Analysis
Sample collection via blood draw or FTA card, performed by a trained professional.
Report Delivery
Sample is sent to the laboratory for DNA extraction and NGS analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the FLVCR2 gene that cause hydranencephaly, Fowler type, aiding in diagnosis, genetic counseling, and family planning.
How to Prepare
- Use sterile collection equipment
- Label samples with patient details accurately
- Store samples at ambient room temperature
- Ensure proper handling to avoid contamination
Doctor's Notes
Reviewed by Dr SHAILAJA RAGHUNATH MURDESHWAR — MBBS, MD (General Medicine) · Reg. No. 8052
"This test is crucial for early diagnosis and genetic counseling in families with a history of hydranencephaly."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Positive
Pathogenic mutation detected in the FLVCR2 gene, confirming diagnosis of hydranencephaly, Fowler type. Genetic counseling is recommended.
Negative
No pathogenic variants found in the FLVCR2 gene. Clinical correlation is advised, as symptoms may be due to other causes.
If symptoms such as seizures, developmental delays, or impaired vision are present, or if there is a family history of hydranencephaly, consult a genetic counselor or healthcare professional for evaluation and testing.
Frequently Asked Questions
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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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