Hereditary Persistence of Fetal Hemoglobin HPFH
Introduction
The Hereditary Persistence of Fetal Hemoglobin (HPFH) test is a genetic examination that plays a pivotal role in identifying individuals who have a condition characterized by the continued production of fetal hemoglobin beyond infancy. This test is essential for diagnosing various hemoglobinopathies and guiding treatment options for patients. Understanding HPFH is crucial for proactive health management, particularly for those with a family history of hemoglobin disorders.
What the Test Measures
The HPFH test measures the levels of fetal hemoglobin (HbF) in the blood. Elevated HbF levels can indicate the presence of genetic mutations that affect hemoglobin production. By analyzing samples such as amniotic fluid, chorionic villi, or cord blood, healthcare providers can gain insights into the patient’s genetic makeup and potential health implications.
Who Should Consider This Test
This test is recommended for individuals who exhibit symptoms such as:
- Chronic anemia
- Family history of sickle cell disease or thalassemia
- Unexplained fatigue or weakness
- Individuals planning to become pregnant or those currently pregnant
Risk factors include a family history of hemoglobin disorders, particularly in populations where such conditions are prevalent.
Benefits of Taking the Test
Taking the HPFH test offers numerous benefits, including:
- Early detection of potential genetic disorders
- Informed decision-making regarding family planning
- Guidance for treatment options and lifestyle adjustments
- Peace of mind for individuals with a family history of hemoglobinopathies
Understanding your genetic health can empower you to take proactive steps towards better health outcomes.
Understanding Your Results
Results from the HPFH test will indicate whether fetal hemoglobin levels are elevated. A healthcare provider will help interpret these results, providing guidance on any necessary follow-up actions or treatments based on the findings.
Test Information
| Test Name | Regular Price | Discount Price |
|---|---|---|
| Hereditary Persistence of Fetal Hemoglobin HPFH | 160,000 NGN | 120,000 NGN |
Booking the Test
To book the Hereditary Persistence of Fetal Hemoglobin (HPFH) test, please contact us at +2348077798758. Our team is ready to assist you with your booking and provide further information.
Important Pre-Test Instructions
The HPFH test can be conducted with a Doctor’s prescription. Please note that a prescription is not applicable for surgery and pregnancy cases or individuals planning to travel abroad.
Sample Type & Components
Sample types for the HPFH test include:
- Amniotic fluid
- Chorionic villi
- Cord blood
Test components required:
- Sterile container
- Sterile Normal Saline Container
- EDTA Vacutainer (2ml)
Turnaround Time
The typical turnaround time for receiving results is approximately 7-8 days.
For further inquiries or to book your test, please reach out to us at +2348077798758.
