Neuro-genetic Testing Test for families from Nandyal
Whole-exome and targeted gene panels for inherited neurological disorders.
Neuro-genetic testing identifies genetic causes of epilepsy, regression, developmental delay and neuromuscular disease. We help families choose the right test - single gene, panel, or whole-exome sequencing - interpret variants, and translate results into a practical plan, including treatment options and family screening.
Quick Appointment
Takes less than 1 minute
What does this test help evaluate?
Unexplained or drug-resistant epilepsy
Suspected inherited neuromuscular disease
Regression of skills or family history
When is this test recommended?
This diagnostic test is not automatically required for every child. The decision to recommend the test is made by the pediatric neurologist after evaluating the child's detailed clinical history and symptoms.
What happens during the test?
A simple blood sample is sent to a partner laboratory.

How to prepare your child
How results are used
Diagnostic results are interpreted in correlation with clinical history, developmental timeline, and symptoms. A diagnostic report by itself does not confirm a complete care plan.
Why specialist interpretation matters
Interpretation by a DM-trained Pediatric Neurologist ensures subtle anomalies are identified accurately, preventing misdiagnosis of non-epileptic mimics.
Where is the test available?
The equipment is located in our Kurnool clinic. We coordinate schedules for families from Nandyal to complete tests and receive reports on the same day.
Related Conditions
Test FAQs
Q. How much does neuro-genetic testing cost, and are gene panels covered?
Neuro-genetic pricing varies widely depending on whether targeted panels, clinical exomes, or whole-exome sequencing is ordered. We partner with leading molecular labs to provide testing at highly subsidized clinical rates.
Has a Neuro-genetic Testing been recommended for your child?
Contact the clinic to confirm preparation instructions, slots, pricing, and timing details.