Diagnostic Laboratory Services
Essential Testing for Accurate Diagnosis and Better Pediatric Care
Diagnostic Laboratory Services play a vital role in understanding your child’s health and guiding effective treatment plans. These tests help uncover underlying medical conditions—especially those that aren’t visible at first glance—and provide clarity for parents and doctors to make informed decisions.
At Dr. Nikhil Pawar’s clinic, specialized diagnostic testing such as genetic and metabolic testing is offered to support children with developmental delays, neurological symptoms, or unexplained health concerns.
Why Are Diagnostic Laboratory Services Important?
Some pediatric health conditions—particularly neurological or developmental ones—can be complex and difficult to diagnose through observation alone. Laboratory testing provides deeper insights that help confirm diagnoses, identify causes, and prevent future complications.
By using advanced testing methods, such as genetic and metabolic evaluations, the clinic can:
- Detect conditions early, even before symptoms become severe
- Pinpoint inherited or metabolic disorders that might be affecting your child’s development
Personalize treatment plans to meet your child’s unique needs
Key Diagnostic Tests Offered
Genetic Testing
What It Is:
Genetic testing helps identify inherited conditions or genetic disorders that may be contributing to your child’s symptoms. This test is especially useful in cases of developmental delays, physical abnormalities, or family history of similar issues.
What to Expect:
A small blood or saliva sample is collected and sent to a laboratory for detailed analysis. Once the results are available, Dr. Pawar explains them clearly and discusses how they may relate to your child’s health.
Metabolic Testing
What It Is:
Metabolic testing examines how your child’s body is converting food into energy. It can reveal enzyme deficiencies or imbalances that might affect growth, brain function, or overall well-being.
What to Expect:
A blood sample is taken to measure various biochemical markers. The results help assess whether your child has a metabolic disorder, and whether treatment or dietary adjustments are needed.
How the Diagnostic Process Works
- Schedule the Test
Appointments for diagnostic tests can be easily booked through the clinic’s reception or consultation team. - Sample Collection
Depending on the test, a blood or saliva sample is collected in a child-friendly and gentle manner. - Lab Analysis
Samples are processed in a certified laboratory. Once complete, results are sent back to the clinic for detailed review. - Consultation & Care Plan: Dr. Pawar discusses the results with you in simple terms, explains any findings, and outlines the next steps for treatment or further investigation.
How Our Diagnostic Lab Benefits Families
- Timely Answers: Our in-house lab speeds up the diagnostic process, helping you avoid delays and get the clarity you need for your child’s care.
- Comprehensive Pediatric Testing: From neurological assessments to routine screenings, we offer a wide range of tests designed specifically for children.
- Stress-Free Experience: Our child-friendly approach helps reduce anxiety during sample collection and testing, making the process easier for both you and your child.
- Expert Guidance: Dr. Pawar ensures that every test result is thoroughly explained so you understand the findings and feel confident about the next steps.
- Integrated Care: Our diagnostic results are seamlessly incorporated into your child’s overall treatment plan, ensuring that every detail supports effective care.
Benefits of Diagnostic Laboratory Services
- Accurate and Reliable Results
Laboratory testing provides concrete answers to help guide care with confidence. - Early Detection of Hidden Issues
Identifying conditions before they progress allows for more effective treatment - Personalized Treatment Planning
Results help tailor medications, therapies, or lifestyle changes specific to your child’s condition. - Peace of Mind for Parents : Understanding what’s happening behind the scenes provides clarity and reduces uncertainty.
Before and After Your Diagnostic Test:
- Before the Test: Depending on the type of test, your child may need to fast or avoid certain foods. We’ll provide specific instructions to help you prepare.
- During the Test: Our team will walk you and your child through each step to reduce stress and explain what to expect. For tests like EEGs, we use simple instructions to help your child stay calm and cooperative.
- After the Test: Once the test is complete, Dr. Pawar will review the results with you during your follow-up consultation and discuss any additional steps needed, such as lifestyle adjustments or treatments.
What to Expect During Testing
The diagnostic experience is designed to be as smooth and stress-free as possible for children and parents:
- Friendly, trained staff make the testing environment calm and reassuring
- All procedures are done with care, using child-appropriate methods
- Parents are kept fully informed at every stage
- Once results are in, Dr. Pawar takes the time to explain everything clearly, answer your questions, and offer guidance on next steps
Whether your child has a known condition or you’re looking for answers to ongoing concerns, diagnostic testing can play a key role in uncovering the cause and building a clear path forward.
4. Diagnostic Laboratory Services – FAQs
These tests help identify underlying causes of symptoms like developmental delays, seizures, or unexplained health concerns, especially when no clear diagnosis is available through physical examination alone.
No. Most tests require a small sample of blood or saliva. The process is safe, and our trained team ensures your child feels comfortable during sample collection.
It depends on the test type. Genetic and metabolic tests typically take between 1 to 3 weeks. The clinic will inform you once results are available for review.
Dr. Pawar will personally review the results with you, explain the findings in simple terms, and recommend the best course of action for treatment or further evaluation.
Yes. Early detection through these tests can help prevent complications by guiding timely and appropriate treatment, improving your child’s long-term health outlook.
