YWHAE Gene Miller Dieker Lissencephaly Syndrome NGS Genetic DNA Test
Introduction
The YWHAE Gene Miller Dieker Lissencephaly Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to identify genetic mutations associated with lissencephaly syndrome. This condition, characterized by abnormal brain development, can lead to a range of neurological issues. Early detection through this test can significantly impact the management and treatment of affected individuals.
What Does the Test Measure?
This test analyzes the YWHAE gene, which plays a crucial role in brain development. By utilizing Next-Generation Sequencing (NGS) technology, the test can detect mutations that may lead to lissencephaly syndrome. It provides comprehensive insights into the genetic factors contributing to this condition.
Who Should Consider This Test?
Parents or guardians should consider this test if their child exhibits symptoms such as:
- Developmental delays
- Seizures
- Abnormal muscle tone
- Distinctive facial features
Additionally, families with a history of genetic disorders or those concerned about dysmorphology should seek this test for a clearer understanding of their child’s health.
Benefits of Taking the Test
- Early diagnosis can lead to timely interventions.
- Informed family planning for future pregnancies.
- Access to specialized medical care and support.
- Peace of mind through understanding genetic risks.
Understanding Your Results
Results from the YWHAE Gene Miller Dieker Lissencephaly Syndrome NGS Genetic DNA Test will provide valuable insights into the genetic status of the individual tested. A genetic counselor will help interpret these results, discussing implications for treatment and management options.
Test Pricing
| Price Type | Price (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To book the YWHAE Gene Miller Dieker Lissencephaly Syndrome NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Ensure your child’s health by taking this important step today!
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 the YWHAE gene.
This test falls under the Pediatrics specialty, in the Genetics department, and employs NGS technology to diagnose dysmorphology-related conditions.
