MYCN Gene Feingold Syndrome NGS Genetic DNA Test
Introduction
The MYCN Gene Feingold Syndrome NGS Genetic DNA Test is an advanced diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to identify mutations in the MYCN gene. This test is crucial for diagnosing Feingold syndrome, a genetic disorder characterized by a range of developmental and physical anomalies. Early detection through this test can significantly enhance patient management and treatment options.
What the Test Measures
This genetic test specifically measures mutations in the MYCN gene, which are associated with Feingold syndrome. By analyzing the genetic material, the test provides insights into the presence of these mutations, allowing for a better understanding of the patient’s condition.
Who Should Consider This Test
Individuals who may benefit from the MYCN Gene Feingold Syndrome NGS Genetic DNA Test include:
- Patients exhibiting symptoms of Feingold syndrome, such as developmental delays, dysmorphic features, and other related anomalies.
- Individuals with a family history of Feingold syndrome or other genetic disorders.
- Patients referred by healthcare providers for genetic counseling.
Benefits of Taking the Test
- Early diagnosis and intervention can lead to improved management of symptoms.
- Understanding genetic predispositions helps in making informed healthcare decisions.
- Provides valuable information for family planning and genetic counseling.
Understanding Your Results
Results from the MYCN Gene Feingold Syndrome NGS Genetic DNA Test are typically available within 3 to 4 weeks. A genetic counselor will assist in interpreting the results, providing guidance on the implications of any identified mutations, and discussing potential next steps in management and treatment.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| MYCN Gene Feingold Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
To take the next step in understanding your genetic health, book the MYCN Gene Feingold Syndrome NGS Genetic DNA Test today. For inquiries or to schedule your appointment, call or WhatsApp us at +2348077798758.
Pre-Test Instructions
Prior to the test, patients should provide a clinical history and participate in a genetic counseling session to create a pedigree chart of family members affected by MYCN Gene Feingold syndrome.
Specialty and Department Information
This test is conducted under the Pediatrics specialty in the Genetics department, utilizing NGS technology to ensure accurate and reliable results for patients suspected of having dysmorphology related to Feingold syndrome.
