HBG2 Gene Cyanosis Transient Neonatal NGS Genetic DNA Test
Introduction
The HBG2 Gene Cyanosis Transient Neonatal NGS Genetic DNA Test is a groundbreaking diagnostic tool that plays a crucial role in identifying genetic anomalies linked to cyanosis in newborns. This test utilizes advanced Next Generation Sequencing (NGS) technology to provide a comprehensive analysis of the HBG2 gene, which is essential in the production of hemoglobin. Understanding the genetic basis of cyanosis can lead to timely interventions and improved health outcomes for affected infants.
What the Test Measures
This test detects mutations in the HBG2 gene that may cause transient neonatal cyanosis. By analyzing the DNA from a blood sample or extracted DNA, healthcare providers can determine whether a newborn has inherited any genetic variations that could lead to complications.
Who Should Consider This Test
Parents with a family history of hemoglobin disorders or those whose newborns exhibit symptoms such as bluish discoloration of the skin (cyanosis) should consider this test. Additionally, infants who have experienced respiratory distress or low oxygen levels may benefit from genetic testing to identify underlying causes.
Benefits of Taking the Test
- Early identification of potential genetic disorders.
- Guidance for treatment options and management strategies.
- Peace of mind for families with a history of genetic conditions.
- Informed decision-making regarding the health of the newborn.
Understanding Your Results
Once the test is completed, results will be provided to the healthcare provider, who will explain the findings and their implications. It is essential to understand that not all genetic mutations lead to health issues, and further counseling may be required to discuss the results in detail.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To ensure your newborn’s health and well-being, book the HBG2 Gene Cyanosis Transient Neonatal NGS Genetic DNA Test today. For more information or to schedule an appointment, please call or WhatsApp us at +2348077798758.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient who is going for the HBG2 Gene Cyanosis Transient Neonatal NGS Genetic DNA Test is required. A genetic counseling session to draw a pedigree chart of family members affected with HBG2 Gene Cyanosis is recommended.
Consult with a hematologist or genetic specialist to learn more about this vital test and its implications for your family’s health.
