IFT122 Gene Cranioectodermal Dysplasia Type 1 NGS Genetic DNA Test
Introduction
The IFT122 Gene Cranioectodermal Dysplasia Type 1 NGS Genetic DNA Test is a state-of-the-art diagnostic tool designed to identify genetic mutations associated with cranioectodermal dysplasia. This condition affects the development of the skull and facial features, leading to a range of physical and health challenges. By utilizing Next-Generation Sequencing (NGS) technology, this test offers unparalleled accuracy and insight into the genetic underpinnings of this disorder.
What the Test Measures
This genetic test specifically measures mutations in the IFT122 gene, which are linked to cranioectodermal dysplasia. By analyzing the DNA from a blood sample or extracted DNA, the test can detect these mutations, providing crucial information for diagnosis and management.
Who Should Consider This Test?
Individuals who may benefit from the IFT122 Gene Cranioectodermal Dysplasia Type 1 NGS Genetic DNA Test include:
- Patients exhibiting symptoms of cranioectodermal dysplasia, such as abnormal skull shape or facial features.
- Families with a history of genetic disorders or craniofacial abnormalities.
- Individuals with risk factors, including known mutations in related genes.
Benefits of Taking the Test
Taking the IFT122 Gene Cranioectodermal Dysplasia Type 1 NGS Genetic DNA Test offers numerous benefits:
- Accurate diagnosis of cranioectodermal dysplasia.
- Informed decision-making regarding treatment and management options.
- Family planning insights for individuals with a family history of the disorder.
- Access to genetic counseling for a deeper understanding of results.
Understanding Your Results
Once the test is completed, results will be communicated to you. It’s important to consult with a genetic counselor or healthcare provider to interpret the results accurately. They will guide you through what the findings mean for your health and your family.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the IFT122 Gene Cranioectodermal Dysplasia Type 1 NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Our team is ready to assist you in scheduling your appointment and answering any questions 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 is required, along with a genetic counseling session to create a pedigree chart of affected family members.
Specialty: Pediatrics | Department: Genetics | Method: NGS Technology | Disease Type: Dysmorphology
