TSC2 GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited    
TSC2 Gene Panel by NGS is a specialized genetic test that detects mutations in the TSC2 gene, which are associated with Tuberous Sclerosis Complex (TSC), a multisystem disorder causing benign tumor growth in various organs. This test helps in confirming the clinical diagnosis, evaluating the severity of disease, and guiding management and family counseling. It is especially useful in individuals presenting with seizures, developmental delay, skin lesions, kidney angiomyolipomas, or cardiac rhabdomyomas. Early genetic detection enables timely treatment and monitoring to prevent complications

  • 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


Booking Procedure:
  1. Technician from Metropolis will be assigned for a home sample collection after booking confirmation.
  2. Sample will be collected by our technician at your address at given slot.
  3. You can make the payment to the technician at the time of collection
  4. Your sample will then be transported to the nearest collection center and will be centrifuged before sending to the lab for processing.
  5. Soft copy reports will be sent to your email address within 24 to 48 hours or as per defined TAT for Tests.

Frequently Asked Questions (FAQ's):

What is the purpose of the TSC2 Gene Panel test?
This test identifies genetic mutations in the TSC2 gene to confirm Tuberous Sclerosis Complex and assess risk for disease-related complications.

Who should consider this test?
Individuals with symptoms such as recurrent seizures, cognitive impairment, skin manifestations, or tumors in the brain, kidneys, lungs, or heart should undergo this test.

What sample type is required?
An EDTA blood sample is required for Next Generation Sequencing (NGS).

How long does the report take?
Results typically take around 2–4 weeks, depending on laboratory workflow.

Can this test help in treatment or prognosis?
Yes, identifying the mutation supports clinical decision-making, targeted therapies (like mTOR inhibitors), and genetic counseling for family planning.

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