Hemoglobinopathy Newborn Screen Test
Introduction
The Hemoglobinopathy Newborn Screen Test is a crucial diagnostic tool aimed at identifying genetic blood disorders in newborns. Early detection of these conditions is vital for effective management and treatment, potentially saving lives and improving the quality of life for affected individuals. This test is particularly important in regions where genetic blood disorders are prevalent.
What the Test Measures
This test measures the presence of abnormal hemoglobin variants in the blood, specifically targeting conditions such as sickle cell disease and thalassemia. By analyzing the hemoglobin patterns, healthcare providers can determine if a newborn is at risk for these genetic disorders.
Who Should Consider This Test
Parents should consider the Hemoglobinopathy Newborn Screen Test if:
- There is a family history of hemoglobin disorders.
- The parents belong to high-risk ethnic groups where these disorders are more common.
- The newborn displays symptoms such as jaundice or anemia.
This test is recommended by pediatricians, gynecologists, and physicians as a standard part of newborn screening.
Benefits of Taking the Test
- Early detection of genetic disorders allows for timely medical intervention.
- Informs parents about potential health risks for their child.
- Facilitates better management of conditions like sickle cell disease and thalassemia.
- Provides peace of mind for families.
Understanding Your Results
Results from the Hemoglobinopathy Newborn Screen Test are typically available the next day. A healthcare provider will discuss the results with you, explaining any abnormalities and the next steps if necessary.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Hemoglobinopathy Newborn Screen Test | 1872 KSh | 2080 KSh |
Test Details
- Turnaround Time: Sample collected on Monday, Wednesday, or Friday by 9 AM; report available the next day.
- Sample Type: 1 drop of heel prick blood on 3 spots of filter paper (available from LPL). Ship refrigerated or frozen. Clinical details and drug history must accompany the sample.
- Pre-Test Instructions: No special preparation required.
- Specialty: Pediatrician, Physician, Gynecologist
- Department: Genetic
- Method: Capillary Electrophoresis
- Disease Type: Genetic Disorders
Book Your Test Today!
We have branches across Kenya and offer home sample collection services for your convenience. To book the Hemoglobinopathy Newborn Screen Test or for more information, please call or WhatsApp us at +254746849631.
