POLYCYSTIC LIVER DISEASE GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited    
The Polycystic Liver Disease Gene Panel by NGS analyzes multiple genes associated with liver cyst formation and related disorders. Metropolis Healthcare performs this test using next-generation sequencing to detect mutations that may contribute to cystic liver disease. It is useful for patients with multiple liver cysts, unexplained hepatomegaly, or a family history of polycystic liver disease. Early genetic diagnosis aids clinicians in monitoring disease progression, planning management, and providing family counseling

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Price: Rs. 21,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0136

Frequently Asked Questions (FAQ's):

What does the Polycystic Liver Disease Gene Panel detect?
It identifies mutations in genes associated with polycystic liver disease and related cystic disorders.

Who should consider this test?
Patients with multiple liver cysts, hepatomegaly, or a family history of polycystic liver disease.

What sample is required?
EDTA blood is used for next-generation sequencing analysis.

How does Metropolis Healthcare perform this test?
Metropolis uses advanced NGS technology to detect both common and rare genetic variants accurately.

Can this test guide treatment decisions?
Yes, it helps clinicians monitor disease progression and plan management strategies.

Is genetic counseling recommended?
Yes, the results provide insights for family members regarding inheritance patterns and risk.

How long does it take to get results from Metropolis Healthcare?
Results are typically available within a few weeks depending on the complexity of the analysis.

Why is early genetic diagnosis important?

It supports timely clinical management, surveillance, and informed family planning 

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