ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test
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ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test

Original price was: KSh 56,000.Current price is: KSh 40,000.

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The ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test is a crucial diagnostic tool for identifying genetic predispositions to central hypoventilation syndrome. Priced at KSh 40,000, this test offers insights into neurological disorders, helping patients and families make informed health decisions. With a turnaround time of 3 to 4 weeks, it is conducted using advanced NGS technology, ensuring accurate and reliable results.

Book your test online and get free home sample collection

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ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test
ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test
KSh 56,000 Original price was: KSh 56,000.KSh 40,000Current price is: KSh 40,000.

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ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test

Introduction

The ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with central hypoventilation syndrome (CHS). This condition, characterized by the inability to control breathing during sleep, can lead to serious health complications. Early detection through genetic testing is crucial for effective management and treatment.

What the Test Measures

This test specifically examines the ASCL1 gene, which is known to play a significant role in the regulation of respiratory function. By analyzing this gene through Next Generation Sequencing (NGS) technology, the test can detect mutations that may indicate a predisposition to CHS.

Who Should Consider This Test?

Individuals who may benefit from this test include:

  • Patients with a family history of central hypoventilation syndrome.
  • Individuals experiencing unexplained respiratory issues, especially during sleep.
  • Those with symptoms such as sleep apnea, fatigue, or difficulty breathing at night.

It is advisable for patients to consult with a neurologist or a genetic counselor to determine if this test is appropriate for their specific situation.

Benefits of Taking the Test

Taking the ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test offers several advantages:

  • Early identification of genetic risks associated with central hypoventilation syndrome.
  • Informed decision-making regarding treatment and management options.
  • Access to tailored genetic counseling and support for affected families.
  • Potential to prevent serious complications through early intervention.

Understanding Your Results

Results from the ASCL1 Gene test will provide insights into the presence of genetic mutations. A genetic counselor will help interpret these results, guiding you through the implications for your health and that of your family members.

Test Pricing

Test Name Discount Price Regular Price
ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test 40,000 KSh 56,000 KSh

Branches and Booking

We have branches across all major cities in Kenya, including Nairobi, Mombasa, and Kisumu. Our team is dedicated to providing you with the highest quality diagnostic services. To book the ASCL1 Gene Central Hypoventilation Syndrome Congenital NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.

For optimal results, prepare for the test by providing a clinical history and considering a genetic counseling session to draw a pedigree chart of family members affected by ASCL1 Gene Central Hypoventilation Syndrome.

Take the first step towards better health today!

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