NAA10 Gene Ogden syndrome NGS Genetic Test
Short Name: NAA10 Ogden NGS
Also known as: Ogden syndrome genetic test, NAA10 gene sequencing, N-terminal acetyltransferase 10 gene test
NAA10 Gene Ogden 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 Reports are delivered within 3-4 weeks after sample receipt.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
The purpose of this test is to confirm or rule out Ogden syndrome in individuals presenting with characteristic clinical features, to aid in early intervention, and to provide genetic counseling for affected families.
- Test Code
- 5875
- CPT Code
- 81407
- ICD Code
- Q87.8
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- Reports are delivered within 3-4 weeks after sample receipt.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No fasting required. A genetic counseling session is recommended to discuss the test and draw a pedigree chart.
Method: Venipuncture or Finger prick
Laboratory Analysis
Blood sample is collected by venipuncture or finger prick onto FTA card. Ensure proper labeling.
Report Delivery
No special precautions. The sample is transported to the lab at ambient temperature.
Timeline: Reports are delivered within 3-4 weeks after sample receipt.
Patient Instructions
About This Test
Who Should Get This Test
The purpose of this test is to confirm or rule out Ogden syndrome in individuals presenting with characteristic clinical features, to aid in early intervention, and to provide genetic counseling for affected families.
How to Prepare
- Use EDTA vacutainer for blood collection
- For FTA card, apply one drop of blood and let it dry
- Label the sample with patient ID and date
- Transport at room temperature
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Ogden syndrome is a rare X-linked disorder primarily affecting males. Early genetic diagnosis is crucial for management and family counseling. NGS provides comprehensive analysis of the NAA10 gene."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted blood sample
- Insufficient sample volume
- Improper labeling
- Sample received after prolonged delay without proper storage
Understanding Your Results
Positive (Pathogenic variant)
Confirms diagnosis of Ogden syndrome. Genetic counseling recommended for family members.
Negative (No variant)
No mutation found in NAA10 gene. Other genetic causes should be considered.
Variant of Uncertain Significance (VUS)
A variant was found but its clinical significance is unknown. Further testing or family studies may be needed.
Consult a clinical geneticist or pediatrician if the child shows developmental delay, dysmorphic features, or unexplained seizures. Genetic counseling is advised before and after testing.
Limitations
- ⚠NGS may not detect large deletions/duplications or deep intronic variants
- ⚠Variant of uncertain significance (VUS) may require further testing
- ⚠Test does not assess other genes associated with similar phenotypes
- ⚠Negative result does not exclude all genetic causes
Risks & Considerations
- ●Minimal risk of bruising or infection at the blood draw site
- ●Psychological impact of receiving a genetic diagnosis
- ●Potential for uncertain results (VUS)
Interfering Factors
- ●Poor DNA quality or quantity
- ●Contamination during sample collection
- ●Recent blood transfusion (may dilute DNA)
- ●Bone marrow transplant (chimerism)
Compare With Similar Tests
| Test | NAA10 Gene Ogden syndrome NGS Genetic Test | Whole Exome Sequencing | Chromosomal Microarray |
|---|---|---|---|
| Comparison | NAA10 Gene Ogden syndrome NGS Genetic Test | WES analyzes all coding regions of the genome, while this test focuses only on the NAA10 gene. WES is more comprehensive but costlier and may take longer. | CMA detects copy number variations, not single-gene mutations. It is useful for detecting large deletions/duplications but not point mutations in NAA10. |
Frequently Asked Questions
What is Ogden syndrome?
How is Ogden syndrome diagnosed?
What is the cost of the NAA10 gene test at DNA Labs India?
What sample is required for the test?
Is fasting required before the test?
How long does it take to get results?
Will I receive raw data files?
Is home sample collection available?
Can females be affected by Ogden syndrome?
What does a positive test result mean?
What if the test result is negative?
Is genetic counseling included?
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₹20,000Reference Laboratory Services
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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