ARX Gene Corpus Callosum Agenesis with Abnormal Genitalia NGS Genetic DNA Test
Introduction
The ARX Gene Corpus Callosum Agenesis with Abnormal Genitalia NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the ARX gene, which can lead to significant neurological and genital abnormalities. This test employs Next-Generation Sequencing (NGS) technology, ensuring a comprehensive analysis of the genetic material. Understanding genetic conditions is vital for early diagnosis and effective management, especially in pediatric patients.
What the Test Measures
This test specifically detects mutations in the ARX gene associated with corpus callosum agenesis and genital abnormalities. By analyzing the DNA, it provides insights into the genetic factors contributing to these conditions, helping clinicians make informed decisions.
Who Should Consider This Test
Individuals exhibiting symptoms such as developmental delays, abnormal genitalia, or neurological issues should consider this test. Additionally, families with a history of similar conditions or those at risk due to genetic factors may benefit from genetic counseling and testing.
Benefits of Taking the Test
- Early diagnosis of genetic conditions.
- Informed decision-making for treatment and management.
- Family planning insights through genetic counseling.
- Access to specialized care in pediatrics and genetics.
Understanding Your Results
Results from the ARX Gene test will indicate the presence of any mutations in the ARX gene. A genetic counselor will help interpret these results, providing guidance on the implications for health and family planning.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| ARX Gene Corpus Callosum Agenesis with Abnormal Genitalia NGS Genetic DNA Test | 400,000 | 560,000 |
Book Your Test Today!
Don’t wait to gain valuable insights into your genetic health. Book the ARX Gene Corpus Callosum Agenesis with Abnormal Genitalia NGS Genetic DNA Test today! For more information, call or WhatsApp us at +2348077798758.
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 undergoing the test and a genetic counseling session to draw a pedigree chart of affected family members are required.
Specialty: Pediatrics | Department: Genetics | Method: NGS Technology | Disease Type: Dysmorphology
