DDX11 Gene Warsaw Breakage Syndrome NGS Genetic DNA Test
Introduction to the DDX11 Gene Warsaw Breakage Syndrome NGS Genetic DNA Test
The DDX11 Gene Warsaw Breakage Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the DDX11 gene, which are associated with Warsaw Breakage Syndrome. This genetic condition is characterized by various physical abnormalities and developmental issues, making early diagnosis crucial for effective management and treatment.
What the Test Measures
This test employs Next Generation Sequencing (NGS) technology to analyze the DDX11 gene. By detecting specific genetic mutations, it helps in understanding the underlying causes of dysmorphology and other related conditions.
Who Should Consider This Test?
Individuals with a family history of Warsaw Breakage Syndrome or those displaying symptoms such as developmental delays, physical abnormalities, or other related dysmorphology signs should consider this test. Risk factors include a known genetic predisposition or previous diagnoses within the family.
Benefits of Taking the Test
- Early and accurate diagnosis of genetic disorders.
- Informed decision-making regarding treatment and management options.
- Enhanced understanding of family health history and genetic risks.
- Access to genetic counseling for better support and guidance.
Understanding Your Results
Results from the DDX11 Gene Warsaw Breakage Syndrome NGS Genetic DNA Test are typically available within 3 to 4 weeks. A genetic counselor will assist you in interpreting the results, explaining what they mean for you and your family, and discussing potential next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
To take the first step towards understanding your genetic health, book the DDX11 Gene Warsaw Breakage Syndrome NGS Genetic DNA Test today. For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758.
Pre-Test Instructions
Prior to the test, it is essential to provide a clinical history and undergo a genetic counseling session. This will help in drawing a pedigree chart of family members affected by the DDX11 gene, ensuring a comprehensive understanding of your genetic background.
Specialty and Department
This test falls under the Pediatrics specialty and is conducted in the Genetics department, utilizing advanced NGS technology to provide accurate results for dysmorphology-related conditions.
