PIGN Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 1 NGS Genetic DNA Test
Introduction
The PIGN Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 1 NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify mutations in the PIGN gene. This test is essential for understanding various genetic disorders that manifest as multiple congenital anomalies, hypotonia, and seizures. By utilizing Next Generation Sequencing (NGS) technology, this test provides a comprehensive analysis of the PIGN gene, aiding in the diagnosis and management of affected individuals.
What the Test Measures
This genetic test specifically measures and detects mutations in the PIGN gene, which is associated with a range of developmental disorders. By analyzing the gene’s sequence, the test can identify potential genetic abnormalities that may lead to serious health issues.
Who Should Consider This Test?
Individuals who should consider the PIGN Gene test include:
- Patients presenting with multiple congenital anomalies
- Individuals with hypotonia (low muscle tone)
- Patients experiencing seizures without a clear etiology
- Families with a history of genetic disorders involving these symptoms
Benefits of Taking the Test
Taking the PIGN Gene test offers numerous benefits, including:
- Accurate diagnosis of genetic conditions
- Guidance for treatment and management options
- Informed family planning and genetic counseling
- Understanding the risk of recurrence in future pregnancies
Understanding Your Results
Upon receiving your test results, a genetic counselor will help interpret the findings. Results may indicate the presence of mutations in the PIGN gene, which can provide insights into the patient’s condition and guide further medical decisions. It is important to discuss these results with a healthcare professional to fully understand their implications.
Test Information and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| PIGN Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 1 NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Don’t wait to gain important insights into your health or the health of your loved ones. To book the PIGN Gene Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 1 NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team at DNA Labs Nigeria is here to assist you with any questions and help you through the booking process.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: Clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by the PIGN gene.
