DNAL4 Gene Mirror movements type 3 NGS Genetic Test
Short Name: DNAL4 Gene Test
Also known as: Congenital Mirror Movements Type 3, DNAL4-related Mirror Movements, Congenital Mirror Movement Disorder
DNAL4 Gene Mirror movements type 3 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 3-4 weeks from sample receipt. 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
The purpose of the DNAL4 Gene Mirror Movements Type 3 NGS Genetic Test is to detect mutations in the DNAL4 gene that cause congenital mirror movements type 3. This test aids in confirming diagnosis, guiding treatment decisions, facilitating genetic counseling, and identifying carriers in families for informed reproductive planning.
- Test Code
- 1716
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3-4 weeks from sample receipt
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
Patient should provide detailed clinical history and family history. A genetic counseling session is recommended to draw a pedigree chart and discuss test implications.
Method: Venipuncture
Laboratory Analysis
Blood sample collected via venipuncture from a vein in the arm. For FTA card, a finger-prick blood sample may be used. The procedure is quick and minimally invasive.
Report Delivery
Apply pressure to the puncture site to stop bleeding. The sample is labeled and sent to the laboratory for analysis. No special post-collection care is required.
Timeline: 3-4 weeks from sample receipt
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the DNAL4 Gene Mirror Movements Type 3 NGS Genetic Test is to detect mutations in the DNAL4 gene that cause congenital mirror movements type 3. This test aids in confirming diagnosis, guiding treatment decisions, facilitating genetic counseling, and identifying carriers in families for informed reproductive planning.
How to Prepare
- Fasting is not required unless specified by the physician.
- Bring identification and test requisition form.
- Inform the phlebotomist of any medications or health conditions.
- Ensure proper labeling of the sample to avoid rejection.
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for DNAL4 mutations is essential for diagnosing congenital mirror movements. It allows for early intervention, personalized management, and informed genetic counseling for families."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Insufficient sample volume
- Hemolyzed or clotted samples
- Unlabeled or mislabeled samples
- Samples with incorrect storage conditions
- Contaminated samples
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis of congenital mirror movements type 3. Genetic counseling and management strategies, such as physical therapy, should be discussed with a specialist.
Negative for pathogenic variant
No mutations detected in DNAL4 gene. Consider other genetic or non-genetic causes. Clinical correlation with symptoms is recommended.
Variant of uncertain significance
A variant was detected but its clinical significance is unknown. Further testing, family studies, or functional assays may be needed for clarification.
If the test result is positive, consult a neurologist or geneticist for management and counseling. If symptoms persist despite negative results, seek further neurological evaluation. For family planning or carrier testing, consult a genetic counselor.
Limitations
- ⚠May not detect all possible mutations in DNAL4 gene
- ⚠Requires genetic counseling for accurate interpretation
- ⚠Results should be correlated with clinical findings
- ⚠Cannot rule out other genetic causes without additional testing
Risks & Considerations
- ●Minor bruising or discomfort at blood draw site
- ●Very rare risk of infection at puncture site
- ●Psychological impact of genetic results, such as anxiety
- ●Potential for variants of uncertain significance causing confusion
Interfering Factors
- ●Sample contamination
- ●Poor DNA quality
- ●Previous blood transfusions
- ●Hemolyzed or clotted samples
- ●Improper sample storage
Compare With Similar Tests
| Test | DNAL4 Gene Mirror movements type 3 NGS Genetic Test | Sanger Sequencing | Array CGH | Whole Exome Sequencing |
|---|---|---|---|---|
| Comparison | DNAL4 Gene Mirror movements type 3 NGS Genetic Test |
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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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