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COMPREHENSIVE OPHTHALMIC GENETIC DISORDER GENE PANEL BY NGS / EDTA BLOOD

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NABL Cap Accredited 
The Comprehensive Ophthalmic Genetic Disorder Gene Panel at Metropolis Healthcare uses Next-Generation Sequencing (NGS) to analyze multiple genes associated with inherited eye disorders. This test helps identify genetic mutations causing congenital or hereditary ophthalmic conditions, enabling early diagnosis, personalized management, and family counseling. Metropolis ensures accurate results using advanced sequencing technology and expert genetic interpretation.

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 21,000.00

Sample Type: EDTA Blood

Fasting Not Requierd


Frequently Asked Questions (FAQ's):

What is the Ophthalmic Genetic Disorder Gene Panel?
It is a genetic test at Metropolis Healthcare that analyzes multiple genes using NGS to detect mutations linked to inherited eye disorders.

Who should consider this test?
Patients with congenital or hereditary eye conditions, unexplained visual impairment, or a family history of ophthalmic disorders may benefit.

What sample is required for this test?
An EDTA blood sample is collected for DNA extraction and NGS analysis at Metropolis Healthcare.

Is fasting required for this test?
No fasting is necessary. The test can be performed without any special preparation.

How accurate are the results from Metropolis Healthcare?
Metropolis ensures high reliability using validated NGS platforms, expert bioinformatics, and strict quality control.

Can this test diagnose eye disorders on its own?
It identifies genetic causes but should be combined with ophthalmological evaluation for a complete diagnosis.

How long does it take to get the results?
Results are typically available within 3–4 weeks, depending on sequencing and analysis at Metropolis Healthcare.

How does this test help in managing ophthalmic disorders?
It aids early diagnosis, guides treatment planning, supports family counseling, and helps predict recurrence risk in siblings or future generations.

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