GLUT1 DEFICIENCY (SLC2A1) GENE PANEL BY NGS, EDTA BLOOD

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The GLUT1 Deficiency (SLC2A1) Gene Panel by NGS is a specialized genetic test that detects mutations in the SLC2A1 gene responsible for GLUT1 Deficiency Syndrome. This rare neurological condition affects glucose transport into the brain, leading to seizures, developmental delays, movement disorders, and cognitive impairment. The test uses an EDTA blood sample and advanced Next Generation Sequencing to deliver highly accurate results. Metropolis Healthcare provides reliable diagnostic insights to support timely treatment decisions, including dietary therapy, and to guide genetic counseling for families 

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Price: Rs. 21,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0118

Frequently Asked Questions (FAQ's):

What is GLUT1 Deficiency Syndrome?
It is a rare neurological disorder caused by reduced glucose transport to the brain due to SLC2A1 gene mutations.

Why is the SLC2A1 gene tested?
Mutations in SLC2A1 are the primary cause of GLUT1 Deficiency Syndrome, making genetic testing important for confirmation.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses advanced NGS technology to accurately detect SLC2A1 gene variants.

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

Who should consider this test?
Individuals with early-onset seizures, developmental delay, abnormal movements, or suspected metabolic brain disorders may benefit from testing.

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

How long do results take at Metropolis Healthcare?
Results are typically available within a few working days depending on laboratory processing.

How can the results help?

They support accurate diagnosis, guide dietary and clinical management, and assist in genetic counseling for families 

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