Neuro-genetic Testing
Whole-exome and targeted gene panels for inherited neurological disorders.
“Identifies genetic causes of epilepsy, regression, developmental delay and neuromuscular disease.”
ఎపిలెప్సీ, రిగ్రెషన్, అభివృద్ధి ఆలస్యం మరియు న్యూరోమస్క్యులర్ వ్యాధి యొక్క జెనెటిక్ కారణాలను గుర్తిస్తుంది.
A simple blood sample is sent to a partner laboratory.
Answers to key parent questions
Is this test safe and painless?
Yes. All our diagnostic tests use child-safe equipment. Non-invasive surface electrodes are used wherever possible.
Is sedation used?
Most tests do not require sedation. We use parent-cooperation strategies and child-friendly distraction techniques.
How long does it take?
Most tests are completed within 20 to 45 minutes.
Are reports available same-day?
Yes. We process and deliver all reports on the same day, allowing out-of-town families to consult Dr. Swetha and head home.
Who is this for?
- Unexplained developmental delay, speech delays, or autism spectrum features
- Intractable or drug-resistant epilepsy starting in infancy or early childhood
- Suspected hereditary neuromuscular diseases (like muscular dystrophies or spinal muscular atrophy)
- Family history of early neurological disorders, regression, or genetic conditions
What to bring with you
- Detailed family health tree information (pedigree details of parents and relatives)
- All previous brain scans (MRI), EEGs, or metabolic screenings
- Information on any birth complications or developmental milestones timeline
Steps in your consultation process
Questions parents commonly ask
How is neuro-genetic testing coordinated?
We partner with leading molecular labs to coordinate genetic testing. After receiving the sequencing reports, our pediatric neurologist provides detailed genetic counseling to explain the variants and structure a care plan.
Ready to schedule Neuro-genetic Testing?
Get same-day bookings, advanced diagnostics performed in-centre, and a detailed written care plan in your language.
Quick Appointment
Takes less than 1 minute