PULMONARY ALVEOLAR MICROLITHIASIS (SLC34A2) GENE PANEL BY NGS, EDTA BLOOD

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The Pulmonary Alveolar Microlithiasis (SLC34A2) Gene Panel by NGS detects mutations in the SLC34A2 gene associated with rare lung disorders characterized by calcium phosphate deposits in the alveoli. Metropolis Healthcare uses advanced next-generation sequencing technology to provide accurate identification of genetic variants. This test is valuable for patients with unexplained respiratory symptoms, restrictive lung patterns, or a family history of pulmonary alveolar microlithiasis. Early genetic diagnosis supports clinical management, monitoring, and genetic counseling for affected families 

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Price: Rs. 21,000.00

Sample Type: EDTA Blood

Fasting Not Required


Notes: G0139

Frequently Asked Questions (FAQ's):

What does the Pulmonary Alveolar Microlithiasis Gene Panel detect?
It identifies mutations in the SLC34A2 gene linked to pulmonary alveolar microlithiasis.

Who should take this test?
Patients with unexplained lung symptoms, restrictive pulmonary function, or a family history of the condition.

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

How does Metropolis Healthcare perform this test?
Metropolis employs high-precision NGS technology to detect both common and rare genetic variants.

Can this test guide clinical management?
Yes, results help clinicians plan monitoring, treatment, and follow-up strategies.

Is genetic counseling recommended?
Yes, the test provides important information for family planning and inheritance risk assessment.

How long are results available from Metropolis Healthcare?
Reports are typically available within a few weeks depending on the analysis complexity.

Why is early detection important?
It enables timely intervention, appropriate monitoring, and informed decision-making for patients and families

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