TSC1 & TSC2 Gene Panel by NGS is an advanced genetic test designed to detect mutations in the TSC1 and TSC2 genes, which are responsible for Tuberous Sclerosis Complex (TSC). This inherited disorder can cause benign tumor growth in the brain, kidneys, heart, skin, and other organs. The test provides valuable information for confirming diagnosis, assessing disease severity, and planning targeted treatment options. It is highly recommended for individuals showing neurological symptoms, seizures, developmental delays, or organ-specific tumors. Genetic results also support family screening and counseling
17 Crores+ Samples Processed
World Class Technology Labs
25+ Years of Trust & Experience
Free Home Collection
Price:
Rs. 17,850.00
Sample Type: EDTA BLOOD
Fasting Not Required
Notes: G0152
Frequently Asked Questions (FAQ's):
What is the purpose of the TSC1 & TSC2 Gene Panel test?
It identifies mutations in the TSC1 and TSC2 genes to diagnose Tuberous Sclerosis Complex and evaluate risk for complications.
Who should undergo this test?
Patients presenting with persistent seizures, developmental delays, autism features, kidney cysts or angiomyolipomas, or skin abnormalities should consider this test.
What sample is required?
EDTA blood sample.
How long does the report take?
Reports are typically available within 2–4 weeks.
Can this test guide treatment?
Yes, results assist in clinical decisions, including suitability for mTOR inhibitor therapies and family genetic counseling