NIN Gene Seckel Syndrome Type 7 NGS Genetic DNA Test
Introduction
The NIN Gene Seckel Syndrome Type 7 NGS Genetic DNA Test is a specialized diagnostic tool designed to identify genetic mutations associated with Seckel syndrome, a rare condition characterized by growth retardation and intellectual disability. This test plays a crucial role in understanding the genetic basis of dysmorphology and helps clinicians provide targeted management for affected individuals.
What the Test Measures
This genetic test utilizes Next-Generation Sequencing (NGS) technology to analyze the NIN gene, which is implicated in Seckel syndrome type 7. By examining the genetic material, the test can detect specific mutations that contribute to the development of this condition.
Who Should Consider This Test
Individuals who should consider the NIN Gene Seckel Syndrome Type 7 NGS Genetic DNA Test include:
- Patients with a family history of Seckel syndrome or related genetic disorders.
- Individuals displaying symptoms such as short stature, microcephaly, and developmental delays.
- Parents seeking genetic counseling for their children with developmental concerns.
Benefits of Taking the Test
The benefits of the NIN Gene Seckel Syndrome Type 7 NGS Genetic DNA Test include:
- Accurate diagnosis of Seckel syndrome, allowing for informed medical decisions.
- Understanding the genetic risks for family members, aiding in family planning.
- Access to targeted therapies and interventions that can improve quality of life.
Understanding Your Results
Results from the NIN Gene Seckel Syndrome Type 7 NGS Genetic DNA Test will provide insights into the presence of mutations in the NIN gene. A genetic counselor will help interpret the results, discussing implications for the patient and their family.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| NIN Gene Seckel Syndrome Type 7 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
To book the NIN Gene Seckel Syndrome Type 7 NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you in scheduling your test and answering any questions you may have.
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test includes blood or extracted DNA, or one drop of blood on an FTA card. Prior to the test, a genetic counseling session is recommended to gather the clinical history of the patient and draw a pedigree chart of family members affected by the NIN gene.
