ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test
Introduction
The ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the ASCL1 gene that are associated with congenital central hypoventilation syndrome (CCHS). This condition affects the body’s ability to regulate breathing, particularly during sleep, leading to serious health risks if left undiagnosed.
What the Test Measures
This test utilizes Next-Generation Sequencing (NGS) technology to analyze the ASCL1 gene. It detects specific genetic variations that may indicate a predisposition to CCHS, helping healthcare providers make informed decisions regarding diagnosis and treatment.
Who Should Consider This Test
Individuals who experience symptoms such as:
- Severe sleep apnea
- Unexplained hypoventilation
- Family history of congenital central hypoventilation syndrome
Patients with risk factors, such as a familial history of neurological disorders, should also consider this test for early diagnosis and management.
Benefits of Taking the Test
- Early identification of congenital central hypoventilation syndrome.
- Informed decision-making for treatment and management strategies.
- Potential for improved quality of life through timely intervention.
- Genetic counseling and support for affected families.
Understanding Your Results
Results from the ASCL1 Gene test will provide insights into the presence of mutations that could lead to congenital central hypoventilation syndrome. A genetic counselor will help interpret the results and discuss the implications for you and your family.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book Your Test Today!
Don’t wait for symptoms to worsen. Book the ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test today for just 400,000 NGN. Call or WhatsApp us at +2348077798758 to schedule your appointment.
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 and a genetic counseling session to draw a pedigree chart of family members affected with ASCL1 Gene Central Hypoventilation Syndrome.
- Specialty: Neurology
- Department: Genetics
- Method: NGS Technology
- Disease Type: Neurological Disorders
