EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test
Introduction to the EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test
The EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to identify mutations in the EFNB1 gene. This test is crucial for diagnosing craniofrontonasal syndrome, a genetic condition that affects facial and cranial development, leading to various physical anomalies.
What the Test Measures
This genetic test specifically measures the presence of mutations in the EFNB1 gene, which are responsible for craniofrontonasal syndrome. By analyzing the genetic material, the test can confirm or rule out the diagnosis, providing essential information for treatment and management.
Who Should Consider This Test?
Individuals who may benefit from the EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test include:
- Patients exhibiting symptoms of craniofrontonasal syndrome, such as facial asymmetry, cleft lip, or other craniofacial abnormalities.
- Individuals with a family history of craniofrontonasal syndrome.
- Parents who have had a child with this condition and are considering future pregnancies.
Benefits of Taking the Test
The benefits of undergoing the EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test include:
- Accurate diagnosis of craniofrontonasal syndrome, allowing for informed medical decisions.
- Identification of genetic predispositions which can guide treatment and management strategies.
- Providing peace of mind for families concerned about hereditary conditions.
Understanding Your Results
Results from the EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test will be communicated clearly to the patient. A genetic counselor will help interpret the findings, explaining whether mutations were detected and what that means for the patient and their family.
Pricing Information
| Test Name | Discount Price | Regular Price |
|---|---|---|
| EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Sample Type and Turnaround Time
The EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test can be performed using:
- Blood or Extracted DNA
- One drop of blood on an FTA card
The turnaround time for results is approximately 3 to 4 weeks.
Pre-Test Instructions
Before taking the test, patients should provide a clinical history and may be required to undergo a genetic counseling session to create a pedigree chart of family members affected by craniofrontonasal syndrome.
Book Your Test Today!
We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. For your convenience, we also offer home sample collection services. Don’t wait—book the EFNB1 Gene Craniofrontonasal Syndrome NGS Genetic DNA Test today! Call or WhatsApp us at +254711564616.
