POLG GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited    
This test analyzes the POLG gene using Next Generation Sequencing (NGS) to detect mutations associated with mitochondrial disorders. It helps diagnose conditions such as progressive external ophthalmoplegia, Alpers syndrome, and other POLG-related neurological disorders. Metropolis Healthcare uses advanced NGS technology to provide accurate and comprehensive genetic insights. The results support early diagnosis, personalized care planning, and informed genetic counseling

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

Price: Rs. 17,850.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: P0165

Frequently Asked Questions (FAQ's):

What does the POLG Gene Panel test check for?
It identifies mutations in the POLG gene that cause various mitochondrial and neurodegenerative disorders.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-depth NGS platforms to deliver precise and reliable genetic results.

Who should consider taking this test?
Individuals with unexplained neurological symptoms, muscle weakness, seizures, or suspected mitochondrial disease may benefit from this test.

What sample is required for the analysis?
A blood sample collected in an EDTA vial is needed for NGS testing.

Is fasting required before giving the sample?
No fasting or special preparation is necessary for this genetic test.

How can this test help in treatment planning?
Accurate detection of POLG mutations helps doctors tailor management strategies and monitor disease progression.

Can family members also be tested?
Yes, Metropolis Healthcare offers family testing and genetic counseling for inherited POLG variants.

How long does it take to receive results?

Genetic tests typically take longer; Metropolis Healthcare provides results within the standard NGS reporting timeline 

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