HLCS Gene Holocarboxylase Synthetase Deficiency NGS Genetic DNA Test
Introduction
The HLCS Gene Holocarboxylase Synthetase Deficiency NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next Generation Sequencing (NGS) technology to identify mutations in the HLCS gene, which are linked to metabolic disorders. This test is vital for individuals who may be at risk of developing conditions related to holocarboxylase synthetase deficiency, a rare metabolic disorder that can lead to serious health complications.
What the Test Measures
This genetic test specifically detects mutations in the HLCS gene, which is responsible for producing an enzyme crucial for the metabolism of certain amino acids and fatty acids. A deficiency in this enzyme can result in the accumulation of toxic substances in the body, leading to a range of metabolic issues.
Who Should Consider This Test
Individuals who should consider the HLCS Gene Holocarboxylase Synthetase Deficiency NGS Genetic DNA Test include:
- Those with a family history of metabolic disorders.
- Patients exhibiting symptoms such as developmental delays, neurological issues, or unexplained metabolic disturbances.
- Individuals undergoing genetic counseling for hereditary conditions.
Benefits of Taking the Test
Taking the HLCS Gene Holocarboxylase Synthetase Deficiency NGS Genetic DNA Test offers numerous benefits, including:
- Accurate diagnosis of metabolic disorders, enabling timely intervention.
- Informed decision-making regarding treatment options and management strategies.
- Understanding genetic risks for family members.
- Access to specialized care and support for affected individuals.
Understanding Your Results
Results from the HLCS Gene Holocarboxylase Synthetase Deficiency NGS Genetic DNA Test will be reviewed by a qualified healthcare professional. It is essential to discuss the findings in the context of your clinical history and symptoms. Positive results indicating a mutation may require further testing or a referral to a genetic specialist.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| HLCS Gene Holocarboxylase Synthetase Deficiency NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Book the Test
To book the HLCS Gene Holocarboxylase Synthetase Deficiency NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with any inquiries and guide 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 holocarboxylase synthetase deficiency.
For more information about this test or other services, visit our website or contact our office.
