MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant NGS Genetic DNA Test
Introduction
The MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant NGS Genetic DNA Test is a cutting-edge diagnostic tool that identifies genetic predispositions associated with Klippel-Feil syndrome. This condition is characterized by the fusion of cervical vertebrae, which can lead to various physical and neurological complications. Understanding your genetic makeup is crucial for early diagnosis and management of this syndrome.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to analyze the MEOX1 gene, which is linked to Klippel-Feil syndrome. It detects mutations that may increase the risk of developing this autosomal dominant condition.
Who Should Consider This Test?
Individuals with a family history of Klippel-Feil syndrome or those displaying symptoms such as a short neck, limited range of motion, or other skeletal anomalies should consider this test. Risk factors include:
- Family history of genetic disorders
- Visible physical symptoms
- Previous diagnoses of related conditions
Benefits of Taking the Test
Taking the MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant NGS Genetic DNA Test offers numerous advantages:
- Early diagnosis and intervention
- Informed family planning decisions
- Access to genetic counseling and support
- Enhanced understanding of the condition and its implications
Understanding Your Results
Results from the MEOX1 Gene test will provide insights into your genetic risk for Klippel-Feil syndrome. A genetic counselor will help interpret these results, offering guidance on potential next steps and management strategies.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant NGS Genetic DNA Test | 400000 NGN | 560000 NGN |
Book Your Test Today!
Don’t wait to understand your genetic health. Book the MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant NGS Genetic DNA Test today! For more information or to schedule your appointment, call or WhatsApp us at +2348077798758.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical History of Patient required. A Genetic Counselling session to draw a pedigree chart of family members affected with MEOX1 Gene Klippel-Feil syndrome type 2.
- Specialty: Pediatrics
- Department: Genetics
- Method: NGS Technology
- Disease Type: Dysmorphology
