ALPHA 1 ANTITRYPSIN DEFICIENCY GENE PANEL BY NGS / EDTA BLOOD

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NABL Cap Accredited      
The Alpha 1 Antitrypsin (A1AT) Deficiency Gene Panel by NGS analyzes genetic variants in the SERPINA1 gene that can lead to reduced or dysfunctional A1AT protein. Metropolis Healthcare performs this test using next-generation sequencing for precise detection of mutations linked to lung and liver disease. It is valuable for patients with unexplained emphysema, chronic obstructive pulmonary disease (COPD), or liver abnormalities. Early genetic identification supports timely clinical management and family counseling.

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Price: Rs. 22,050.00

Sample Type: EDTA Blood

Fasting Not Required


Notes: G0083

Frequently Asked Questions (FAQ's):

What does the Alpha 1 Antitrypsin Deficiency Gene Panel detect?
It identifies mutations in the SERPINA1 gene associated with A1AT deficiency.

Who should consider this test?
Individuals with early-onset COPD, unexplained liver disease, or a family history of A1AT deficiency.

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 plan appropriate management for lung and liver complications.

Is genetic counseling recommended?
Yes, results can inform family members about potential carrier status or 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 detection important?
Early identification allows preventive care, lifestyle modification, and timely treatment to reduce disease progression

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