TSC1 Gene Panel by NGS is a specialized molecular test that detects pathogenic variants in the TSC1 gene associated with Tuberous Sclerosis Complex (TSC). Mutations in this gene can lead to abnormal cell growth and formation of benign tumors in multiple organs including the brain, kidneys, heart, lungs, and skin. This test helps confirm clinical diagnosis, assess disease severity, and guide targeted treatment strategies. It is valuable for individuals with unexplained seizures, developmental delays, autism spectrum features, or organ-based tumors. The test also supports family screening and genetic counseling
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Price:
Rs. 17,850.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes: G0151
Frequently Asked Questions (FAQ's):
What is the TSC1 Gene Panel used for?
It is used to identify mutations in the TSC1 gene to diagnose Tuberous Sclerosis Complex and assess related clinical risks.
Who should take this test?
Patients with recurrent seizures, neurodevelopmental issues, kidney lesions, or skin abnormalities suggestive of TSC.
What sample is required?
EDTA blood sample.
How long does the report take?
Approximately 2–4 weeks.
Does this help in treatment planning?
Yes, results can guide personalized management and targeted therapy decisions, including use of mTOR inhibitors