LBR Gene Greenberg Skeletal Dysplasia NGS Genetic DNA Test
The LBR Gene Greenberg Skeletal Dysplasia NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify genetic mutations associated with skeletal dysplasia. This test is particularly significant for individuals with symptoms of skeletal abnormalities, providing clarity and direction for further medical management.
What the Test Measures/Detects
This genetic test utilizes Next Generation Sequencing (NGS) technology to analyze the LBR gene, which is implicated in skeletal dysplasia. By detecting mutations within this gene, the test can confirm or rule out diagnoses related to skeletal growth and development disorders.
Who Should Consider This Test
Individuals who exhibit the following symptoms or have risk factors should consider undergoing the LBR Gene Greenberg Skeletal Dysplasia NGS Genetic DNA Test:
- Unexplained skeletal abnormalities
- Family history of skeletal dysplasia
- Growth retardation
- Joint deformities or limitations
Benefits of Taking the Test
Taking the LBR Gene Greenberg Skeletal Dysplasia NGS Genetic DNA Test offers numerous benefits, including:
- Accurate diagnosis of skeletal dysplasia
- Informed decision-making regarding treatment options
- Understanding family risk factors and implications for future generations
- Access to genetic counselling and support services
Understanding Your Results
Results from the LBR Gene Greenberg Skeletal Dysplasia NGS Genetic DNA Test will provide insights into the presence of mutations in the LBR gene. A genetic counsellor will assist in interpreting these results, discussing potential implications for health and treatment.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| LBR Gene Greenberg Skeletal Dysplasia NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today
To ensure timely diagnosis and management, we encourage you to book the LBR Gene Greenberg Skeletal Dysplasia NGS Genetic DNA Test today. For more information or to schedule your appointment, please call or WhatsApp us at +2348077798758. Our dedicated team is here to assist you with any questions or concerns you may have.
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-test Instructions: A clinical history of the patient who is going for the test and a genetic counselling session to draw a pedigree chart of affected family members is required.
Specialty: Pediatrics
Department: Genetics
Method: NGS Technology
Disease Type: Dysmorphology
