SPTB Gene Anemia Neonatal Hemolytic Fatal and Nearfatal NGS Genetic DNA Test
Introduction
The SPTB Gene Anemia Neonatal Hemolytic Fatal and Nearfatal NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic predispositions to severe anemia in newborns. This test is particularly important as it helps in early detection and intervention, potentially saving lives and improving health outcomes for infants at risk of severe hemolytic anemia.
What the Test Measures
This test specifically detects mutations in the SPTB gene, which are associated with neonatal hemolytic anemia. By utilizing Next Generation Sequencing (NGS) technology, the test provides a comprehensive analysis of the genetic material to identify any harmful variations that could lead to serious health complications.
Who Should Consider This Test
Parents with a family history of anemia or those who have had previous children affected by hemolytic anemia should consider this test. Additionally, infants presenting symptoms such as jaundice, lethargy, or pallor should be evaluated for this genetic condition. Risk factors include maternal health issues and genetic predispositions that may affect the child.
Benefits of Taking the Test
- Early diagnosis of potential genetic disorders.
- Informed decision-making regarding treatment options.
- Peace of mind for parents through understanding genetic risks.
- Guidance for future pregnancies and family planning.
Understanding Your Results
Results from the SPTB Gene Anemia test will indicate whether any mutations associated with neonatal hemolytic anemia are present. A genetic counseling session is recommended to help interpret the results and discuss the implications for the infant and family. This can assist in understanding the next steps for treatment or monitoring.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
SPTB Gene Anemia Neonatal Hemolytic Fatal and Nearfatal NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To ensure your child’s health and well-being, book the SPTB Gene Anemia Neonatal Hemolytic Fatal and Nearfatal NGS Genetic DNA Test today! For appointments and inquiries, please call or WhatsApp us at +2348077798758.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood or extracted DNA, or even one drop of blood on an FTA card. Prior to testing, a clinical history of the patient is necessary, along with a genetic counseling session to create a pedigree chart of affected family members.
This test falls under the specialty of Hematology and is conducted in the Genetics department using advanced NGS technology.