CDKN1C Gene Beckwith-Wiedemann Syndrome NGS Genetic DNA Test
Introduction
The CDKN1C Gene Beckwith-Wiedemann Syndrome NGS Genetic DNA Test is a vital diagnostic tool designed to assess genetic predispositions to Beckwith-Wiedemann syndrome (BWS). This condition is characterized by overgrowth, increased risk of tumors, and other related health issues. Understanding your genetic makeup is crucial in managing potential health risks associated with this syndrome.
What the Test Measures
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the CDKN1C gene, which plays a significant role in cell cycle regulation. By detecting mutations or alterations in this gene, the test can help identify individuals at risk for developing BWS and related conditions.
Who Should Consider This Test?
Individuals with a family history of Beckwith-Wiedemann syndrome or related symptoms should consider this test. Symptoms may include:
- Unusual growth patterns
- Abdominal wall defects
- Macroglossia (enlarged tongue)
- Hemihypertrophy (asymmetrical growth of body parts)
Additionally, parents with a history of genetic disorders or those who have had children with BWS may benefit from this testing.
Benefits of Taking the Test
Taking the CDKN1C Gene Beckwith-Wiedemann Syndrome NGS Genetic DNA Test offers several benefits:
- Early detection of genetic predispositions
- Informed decision-making regarding health management
- Potentially guiding treatment options for affected individuals
- Providing valuable information for family planning and genetic counseling
Understanding Your Results
Results from this test will indicate whether any mutations in the CDKN1C gene have been detected. A positive result may necessitate further medical evaluation and monitoring. It is essential to discuss your results with a healthcare provider who can provide guidance on the implications and next steps.
Test Details and Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| CDKN1C Gene Beckwith-Wiedemann Syndrome NGS Genetic DNA Test | 400,000 | 560,000 |
Pre-Test Instructions
Before undergoing the CDKN1C Gene Beckwith-Wiedemann Syndrome NGS Genetic DNA Test, it is recommended to:
- Provide a clinical history of the patient
- Attend a genetic counseling session to draw a pedigree chart of family members affected by BWS
Book Your Test Today!
Don’t wait to understand your genetic risks. Book the CDKN1C Gene Beckwith-Wiedemann Syndrome NGS Genetic DNA Test today! For more information or to schedule your appointment, please call or WhatsApp us at +2348110567037.
