DNPH Urine Test
Introduction to the DNPH Urine Test
The DNPH Urine Test is an essential diagnostic procedure designed to identify inborn errors of metabolism. These metabolic disorders can significantly impact a child’s health and development, making early detection crucial for effective management. By analyzing urine samples for specific metabolic markers, healthcare providers can gain valuable insights into a patient’s metabolic function.
What the DNPH Urine Test Measures
This test measures the presence of dinitrophenylhydrazine (DNPH) derivatives in urine, which are indicative of certain metabolic disorders. By detecting abnormal levels of these compounds, the test can help identify conditions that require further evaluation and management.
Who Should Consider the DNPH Urine Test?
Parents and guardians should consider the DNPH Urine Test for children exhibiting symptoms such as:
- Unexplained developmental delays
- Failure to thrive
- Behavioral changes
- Recurrent vomiting
- Seizures
Additionally, children with a family history of metabolic disorders may benefit from this test as a preventive measure.
Benefits of Taking the DNPH Urine Test
- Early detection of metabolic disorders
- Guides treatment decisions and management plans
- Non-invasive sample collection
- Same-day report turnaround for timely intervention
- Access to expert pediatric care and support
Understanding Your Results
Results from the DNPH Urine Test will indicate whether the levels of DNPH derivatives are within normal ranges. A healthcare provider will interpret the results, considering the patient’s clinical history and symptoms, to determine if further testing or intervention is necessary.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
DNPH Urine Test | 280 KSh | 312 KSh |
Book Your DNPH Urine Test Today!
We have branches across all major cities in Kenya, making it convenient for you to access our services. To book the DNPH Urine Test or for more information, please call or WhatsApp us at +254711564616.
Test Details
- Turnaround Time: Sample Daily by 2 PM; Report Same Day
- Sample Type: 10 mL (5 mL min.) aliquot of first morning urine OR Post feed urine. Ship refrigerated or frozen.
- Pre-Test Instructions: No special preparation required
- Specialty: Pediatrician
- Department: Genetic
- Method: Biochemical
- Disease Type: Inborn errors of metabolism