SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic Test
Short Name: SLC29A3 HLAS NGS Test
Also known as: Histiocytosis-lymphadenopathy plus syndrome, HLAS
SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome 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 3-4 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
The purpose of this test is to identify pathogenic mutations in the SLC29A3 gene to confirm a diagnosis of Histiocytosis-lymphadenopathy plus syndrome (HLAS), guide treatment decisions, and facilitate genetic counseling for affected individuals and their families.
- Test Code
- 4964
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3-4 weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with HLAS are recommended before testing.
Method: Venipuncture or FTA card
Laboratory Analysis
Standard blood draw procedure using venipuncture or collection of a blood drop on an FTA card. No special preparation is required.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Store samples as per instructions for stability.
Timeline: 3-4 weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to identify pathogenic mutations in the SLC29A3 gene to confirm a diagnosis of Histiocytosis-lymphadenopathy plus syndrome (HLAS), guide treatment decisions, and facilitate genetic counseling for affected individuals and their families.
How to Prepare
- No fasting required
- Bring valid ID and prescription
- Ensure sample is properly labeled
- For FTA card, follow specific instructions for blood application
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for HLAS is crucial for early diagnosis and management. Consult with a genetic counselor for family planning and treatment options."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Insufficient sample volume
- Improperly labeled or contaminated samples
Understanding Your Results
No pathogenic variants detected
Negative for SLC29A3 mutations; HLAS unlikely but clinical correlation is advised.
Pathogenic or likely pathogenic variant detected
Confirms diagnosis of HLAS; genetic counseling and treatment planning recommended.
Variant of uncertain significance (VUS)
Further testing or family studies may be needed; clinical management based on symptoms.
Consult a geneticist, immunologist, or dermatologist if symptoms persist, worsen, or if there is a family history of HLAS. Genetic counseling is advised for all positive results.
Limitations
- ⚠May not detect all types of mutations (e.g., large deletions/duplications)
- ⚠Results require interpretation by a genetic counselor or specialist
- ⚠Does not rule out other genetic or non-genetic causes of symptoms
Risks & Considerations
- ●Minimal risk from blood draw (e.g., bruising, infection)
- ●Psychological impact of genetic results
- ●Potential for uncertain results requiring further testing
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Hemolyzed blood sample
Compare With Similar Tests
| Test | SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic Test | Whole Exome Sequencing | Targeted Gene Panel for Immunodeficiency | Sanger Sequencing |
|---|---|---|---|---|
| Comparison | SLC29A3 Gene Histiocytosis-lymphadenopathy plus syndrome NGS Genetic Test |
Frequently Asked Questions
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