Price:
Rs. 21,000.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes: G0096
Frequently Asked Questions (FAQ's):
What conditions are associated with C8ORF37 mutations?
Mutations in the C8ORF37 gene can cause inherited retinal dystrophies, progressive vision loss, and certain ciliopathies.
Which gene is tested in this panel?
The C8ORF37 gene is analyzed for pathogenic variants responsible for retinal and multisystemic disorders.
How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-precision NGS technology to detect deletions, duplications, and point mutations in the C8ORF37 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 progressive vision impairment, retinal dystrophy, or a family history of C8ORF37-related disorders.
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 management of visual symptoms, and provide valuable information for genetic counselling