HEREDITARY FRUCTOSE INTOLERANCE GENE PANEL BY NGS, EDTA BLOOD

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The Hereditary Fructose Intolerance Gene Panel by NGS is a specialized genetic test that detects mutations commonly associated with Hereditary Fructose Intolerance, a rare metabolic disorder that impairs the body’s ability to break down fructose. Symptoms may include vomiting, abdominal pain, hypoglycemia, liver dysfunction, and feeding difficulties triggered by fructose-containing foods. This test is performed using an EDTA blood sample and advanced Next Generation Sequencing for accurate identification of disease-causing variants. Metropolis Healthcare provides reliable diagnostic insights to enable early dietary intervention, clinical management, and genetic counseling for affected families

  • 17 Crores+ Samples Processed
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Price: Rs. 19,950.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0121

Frequently Asked Questions (FAQ's):

What is Hereditary Fructose Intolerance?
It is a rare metabolic disorder in which the body cannot properly process fructose, leading to serious health complications after fructose intake.

Which gene is tested in this panel?
The test analyzes genes associated with fructose metabolism disorders, including the ALDOB gene, which is the primary cause of Hereditary Fructose Intolerance.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses advanced Next Generation Sequencing (NGS) to detect clinically significant mutations with high accuracy.

What sample type is required?
EDTA whole blood is required for genetic analysis.

Who should consider this test?
Individuals with symptoms after consuming fructose, infants with feeding intolerance, or those with a family history of this condition may benefit from testing.

Is any special preparation needed for this test?
No fasting or special preparation is needed.

How long does it take to receive results from Metropolis Healthcare?
Reports are typically available within a few working days depending on laboratory workflow.

How do the results help?
The results confirm diagnosis, guide dietary restrictions, and support genetic counseling for family planning

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