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CONGENITAL CATARACT GENE PANEL BY NGS / EDTA BLOOD

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NABL Cap Accredited 
The Congenital Cataract Gene Panel at Metropolis Healthcare uses Next-Generation Sequencing (NGS) to analyze genes associated with inherited cataracts. This test helps identify genetic mutations causing congenital cataracts, enabling early diagnosis, family counseling, and personalized management. Metropolis ensures precise results through 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 Congenital Cataract Gene Panel?
It is a genetic test at Metropolis Healthcare that analyzes multiple genes using NGS to detect mutations linked to congenital cataracts.

Who should consider this test?
Infants or children with diagnosed or suspected congenital cataracts, or families with a history of inherited eye disorders.

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 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 congenital cataracts on its own?
It identifies genetic causes but should be combined with clinical evaluation and ophthalmological assessment.

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 congenital cataracts?
It aids early diagnosis, guides treatment planning, supports family counseling, and helps predict recurrence risk in siblings or future offspring.

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