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DNA Labs India

Retinal Degeneration Gene Panel Test

DNA Labs India | ISO 9001:2015 Certified

Retinal Degeneration Gene Panel Test

Short Name: Retinal Deg Panel

Also known as: Retinal Dystrophy Gene Panel, Inherited Retinal Disorder Genetic Test

Retinal Degeneration Gene Panel Test test available at DNA Labs India for ₹36,000. Uses Next-Generation Sequencing (NGS) on Amniotic fluid, Chorionic villi, Peripheral blood samples. Results in 4-6 weeks from sample receipt. Free home collection in 300+ cities across India.

Genetic Panel🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Retinal Degeneration Gene Panel is to identify genetic mutations responsible for inherited retinal disorders, enabling precise diagnosis, personalized treatment strategies, and informed genetic counseling for patients and their families.

Test Code
3180
Price
₹36,000
Sample Type
Amniotic fluid, Chorionic villi, Peripheral blood
Result Time
4-6 weeks from sample receipt
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Ensure a doctor's prescription is available. For blood samples, no fasting is required. For amniotic fluid or chorionic villi samples, follow specific prenatal testing guidelines.

Method: Venipuncture for blood, amniocentesis for amniotic fluid, chorionic villus sampling (CVS) for chorionic villi

Step 2

Laboratory Analysis

Blood draw via venipuncture using EDTA vacutainer. For amniocentesis or CVS, procedures are performed by trained healthcare professionals in a clinical setting.

Step 3

Report Delivery

Apply pressure to the puncture site for blood draws. For prenatal samples, monitor for any complications as advised by the healthcare provider.

Timeline: 4-6 weeks from sample receipt

Patient Instructions

1
Before the Test:Obtain a doctor's prescription. No special preparation needed for blood tests. For prenatal samples, follow specific medical advice.
2
During the Test:Sample collection is quick and minimally invasive for blood draws. Prenatal procedures may involve slight discomfort but are performed under medical supervision.
3
After the Test:Resume normal activities. Monitor for any side effects from prenatal procedures as advised.

About This Test

Who Should Get This Test

The purpose of the Retinal Degeneration Gene Panel is to identify genetic mutations responsible for inherited retinal disorders, enabling precise diagnosis, personalized treatment strategies, and informed genetic counseling for patients and their families.

How to Prepare

  • Use sterile containers for sample collection
  • Label samples correctly with patient details
  • Transport samples in cool packs to maintain stability
  • Follow aseptic techniques to prevent contamination

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing for retinal degeneration can guide treatment decisions and inform family planning, especially for inherited conditions."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid, Chorionic villi, Peripheral blood
Sample VolumeVaries based on sample type
ContainerSterile container, Sterile Normal Saline Container, EDTA Vacutainer (3 ml)
Collection MethodVenipuncture for blood, amniocentesis for amniotic fluid, chorionic villus sampling (CVS) for chorionic villi

Sample Stability

Sample Rejection Criteria:
  • Insufficient sample volume
  • Contaminated or hemolyzed samples
  • Improper labeling or missing patient information
  • Samples not stored or transported correctly

Understanding Your Results

Results from the Retinal Degeneration Gene Panel indicate the presence or absence of pathogenic genetic variants. A positive result confirms a genetic basis for retinal degeneration, while a negative result may require further testing or clinical evaluation.
📊

Positive for pathogenic variant

Confirms genetic diagnosis; consider genetic counseling and tailored treatment.

📊

Negative for pathogenic variant

No mutations detected in tested genes; clinical correlation and additional tests may be needed.

📊

Variant of uncertain significance (VUS)

Further research and family studies recommended for clarification.

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms like night blindness, vision loss, or have a family history of retinal disorders. After receiving test results, seek genetic counseling or an ophthalmologist for management options.

Limitations

  • May not detect all genetic variants or novel mutations
  • Results require clinical correlation and genetic counseling
  • Limited to genes included in the panel; not exhaustive for all retinal disorders

Risks & Considerations

  • Minimal risk for blood draws: bruising, infection
  • For amniocentesis/CVS: risk of miscarriage, infection, or cramping (typically <1%)

Interfering Factors

  • Sample contamination during collection or transport
  • Degraded DNA due to improper storage
  • Recent blood transfusions may affect results

Compare With Similar Tests

TestRetinal Degeneration Gene PanelSingle Gene TestWhole Exome SequencingElectroretinography (ERG)Optical Coherence Tomography (OCT)
ComparisonRetinal Degeneration Gene PanelTargets one specific gene; less comprehensive than a panel.Analyzes all protein-coding genes; more extensive but higher cost and longer turnaround.Functional test for retinal activity; complementary to genetic testing.Imaging test for retinal structure; helps assess physical damage.

Frequently Asked Questions

What is the Retinal Degeneration Gene Panel test?
It is a genetic test that analyzes multiple genes associated with inherited retinal disorders to identify mutations causing vision loss.
How much does the test cost?
The test costs INR 36000 at DNA Labs India, with home sample collection included.
What samples are required for the test?
Samples can be peripheral blood, amniotic fluid, or chorionic villi, collected in sterile containers.
Is fasting required before the test?
No, fasting is not required for this test.
How long does it take to get results?
Results are typically available within 4-6 weeks after sample collection.
Is home sample collection available?
Yes, free home collection is available for online bookings across many cities in India.
Do I need a doctor's prescription for the test?
Yes, a prescription is required, except for surgery, pregnancy, or travel abroad cases.
What symptoms indicate the need for this test?
Symptoms like night blindness, loss of peripheral vision, blurred vision, and sensitivity to light may warrant testing.
How is the test performed?
The test uses Next-Generation Sequencing (NGS) to analyze DNA from the provided sample for genetic mutations.
What do the results mean?
Results show if pathogenic variants are detected, helping diagnose retinal degeneration and guide treatment.
Are there any risks associated with the test?
Risks are minimal for blood draws; prenatal procedures carry slight risks like miscarriage, which should be discussed with a doctor.
Can the test detect all types of retinal degeneration?
The panel covers many genes but may not detect all variants; clinical correlation is essential.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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For Hospitals & Clinics

Reference 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.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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