HYPERARGININEMIA (ARG1) GENE PANEL BY NGS, EDTA BLOOD

image not found

NABL Cap Accredited    
The Hyperargininemia (ARG1) Gene Panel by NGS is a specialized genetic test designed to detect mutations in the ARG1 gene responsible for hyperargininemia, a rare urea cycle disorder. The condition leads to elevated arginine levels in the blood, causing developmental delays, seizures, spasticity, and progressive neurological symptoms. Performed using an EDTA blood sample, this test utilizes advanced Next Generation Sequencing for accurate and detailed variant detection. Metropolis Healthcare provides reliable results that support early diagnosis, personalized treatment planning, and informed genetic counseling for families

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

Price: Rs. 19,950.00

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 hyperargininemia?
Hyperargininemia is a rare metabolic disorder caused by high blood arginine levels due to impaired urea cycle function.

Why is the ARG1 gene tested?
Mutations in the ARG1 gene are responsible for hyperargininemia, making genetic testing essential for definitive diagnosis.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses advanced NGS technology to analyze ARG1 gene variants with high precision and reliability.

Which sample is required for this test?
An EDTA whole blood sample is required for analysis.

Who should consider this test?
Individuals with developmental delay, muscle stiffness, seizures, or a family history of urea cycle disorders may benefit from testing.

Is fasting or preparation needed?
No special preparation or fasting is required.

How soon are results available from Metropolis Healthcare?
Results are typically issued within a few working days based on laboratory workflow.

How do the test results help?
They assist in confirming diagnosis, guiding metabolic management, and providing valuable insights for genetic counseling

OUR corporates PARTNER

Feedback

Patient's Testimonials

Trusted by Thousands

OUR Accreditations

OUR Lab