ALEXANDER DISEASE GENE PANEL BY NGS / EDTA BLOOD

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NABL Cap Accredited   
The Alexander Disease Gene Panel by NGS from Metropolis Healthcare analyzes the GFAP gene to detect mutations responsible for Alexander disease, a rare neurodegenerative disorder. The condition leads to developmental delay, spasticity, seizures, macrocephaly, and progressive neurological decline. The test is performed on an EDTA blood sample using advanced Next Generation Sequencing for precise detection of pathogenic variants. Metropolis Healthcare provides accurate results to support early diagnosis, clinical management, and genetic counselling

  • 17 Crores+ Samples Processed
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  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 21,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0089

Frequently Asked Questions (FAQ's):

Alexander Disease is a rare genetic disorder caused by mutations in the GFAP gene, leading to neurological deterioration, developmental delay, and seizures.

Which gene is tested in this panel?
The GFAP gene is analyzed, as mutations in this gene are the primary cause of Alexander Disease.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-precision NGS technology to detect point mutations, deletions, and duplications in the GFAP gene.

What sample type is required?
An EDTA whole blood sample is needed for DNA extraction and sequencing.

Who should consider this test?
Individuals with developmental delay, spasticity, seizures, macrocephaly, or a family history of Alexander Disease.

Is any preparation needed before testing?
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 workflow.

How will the results help?
They confirm diagnosis, guide neurological care, and provide information for genetic counselling and family planning

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