CFC1 Gene Heterotaxy Visceral Type 2 NGS Genetic DNA Test
Introduction
The CFC1 Gene Heterotaxy Visceral Type 2 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the CFC1 gene, which are associated with heterotaxy and other congenital anomalies. This test utilizes Next Generation Sequencing (NGS) technology to provide comprehensive insights into genetic predispositions, aiding in the early diagnosis and management of related conditions.
What the Test Measures
This test specifically detects mutations in the CFC1 gene, which plays a critical role in the proper placement of internal organs. By identifying these mutations, healthcare providers can better understand the genetic basis of heterotaxy and its implications for patient care.
Who Should Consider This Test
Individuals who may benefit from the CFC1 Gene Heterotaxy Visceral Type 2 NGS Genetic DNA Test include:
- Patients with congenital heart defects.
- Individuals with a family history of dysmorphology or congenital anomalies.
- Patients presenting symptoms related to organ placement abnormalities.
Benefits of Taking the Test
- Early diagnosis of genetic conditions.
- Informed decision-making regarding treatment options.
- Identification of familial risk factors, allowing for proactive health management.
- Access to genetic counseling and support.
Understanding Your Results
Results from the CFC1 Gene Heterotaxy Visceral Type 2 NGS Genetic DNA Test will be provided in a clear format, detailing any identified mutations and their implications. It is essential to discuss these results with a healthcare provider or genetic counselor for proper interpretation and guidance on next steps.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| CFC1 Gene Heterotaxy Visceral Type 2 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To schedule your CFC1 Gene Heterotaxy Visceral Type 2 NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website for more information. Take the first step towards understanding your genetic health today!
Additional Information
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 and a genetic counseling session to draw a pedigree chart of family members affected by CFC1 Gene Heterotaxy are required.
This test falls under the specialty of Pediatrics, within the Genetics department, utilizing NGS technology to assess dysmorphology-related diseases.
