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AASS Gene Hyperlysinemia Type 1 Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The AASS Gene Hyperlysinemia Type 1 Genetic Test is a specialized diagnostic tool used to detect mutations in the AASS gene, which are responsible for Hyperlysinemia Type 1, a rare metabolic disorder. This condition is characterized by an excess of the amino acid lysine in the blood, which can lead to various health issues, including developmental delays, seizures, and behavioral problems. The test is crucial for early detection and management of the condition, allowing for appropriate interventions and lifestyle adjustments to mitigate symptoms and improve quality of life.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific genetic mutations in the AASS gene. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed reporting provided by the lab. By identifying individuals with Hyperlysinemia Type 1, this genetic test plays a vital role in personalized medicine, offering affected families the information needed to make informed health and reproductive decisions.

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  • This test is not intended for medical diagnosis or treatment
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AASS Gene Hyperlysinemia type 1 Genetic Test

At DNA Labs UAE, we offer the AASS Gene Hyperlysinemia type 1 Genetic Test. This test is designed to diagnose hyperlysinemia type 1, a rare genetic disorder characterized by elevated levels of lysine in the blood and urine. The test utilizes Next-Generation Sequencing (NGS) technology to analyze the AASS gene for mutations associated with the condition.

Test Details

The AASS gene hyperlysinemia type 1 NGS genetic test is a diagnostic test that utilizes NGS technology to analyze the AASS gene for mutations associated with hyperlysinemia type 1. The test involves extracting DNA from a blood or saliva sample and sequencing the AASS gene to identify any mutations or genetic variants. The results of the test can help confirm a diagnosis of hyperlysinemia type 1 and guide treatment decisions.

Test Components and Price

  • Test Name: AASS Gene Hyperlysinemia type 1 Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the AASS Gene Hyperlysinemia type 1 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with Hyperlysinemia type 1.

About Hyperlysinemia type 1

Hyperlysinemia type 1 is a rare genetic disorder characterized by elevated levels of the amino acid lysine in the blood and urine. It is caused by mutations in the AASS gene, which provides instructions for producing the enzyme aminoadipic semialdehyde synthase. This enzyme is involved in the breakdown of lysine in the body.

NGS Technology

NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive evaluation of genetic variations that may be responsible for hyperlysinemia type 1. This advanced technology enables us to accurately identify any mutations or genetic variants in the AASS gene.

Genetic Counseling

Genetic counseling may be recommended to discuss the implications of the test results and provide information on the inheritance pattern of hyperlysinemia type 1. Our team of experts can guide you through the process and help you understand the results.

Don’t wait any longer. Contact DNA Labs UAE today to schedule your AASS Gene Hyperlysinemia type 1 Genetic Test and get the answers you need.

Test Name AASS Gene Hyperlysinemia type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for AASS Gene Hyperlysinemia type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hyperlysinemia type 1
Test Details

AASS gene hyperlysinemia type 1 NGS genetic test is a diagnostic test that uses Next-Generation Sequencing (NGS) technology to analyze the AASS gene for mutations associated with hyperlysinemia type 1.

Hyperlysinemia type 1 is a rare genetic disorder characterized by elevated levels of the amino acid lysine in the blood and urine. It is caused by mutations in the AASS gene, which provides instructions for producing the enzyme aminoadipic semialdehyde synthase. This enzyme is involved in the breakdown of lysine in the body.

NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive evaluation of genetic variations that may be responsible for hyperlysinemia type 1. The test involves extracting DNA from a blood or saliva sample and sequencing the AASS gene to identify any mutations or genetic variants.

The results of the test can help confirm a diagnosis of hyperlysinemia type 1 and guide treatment decisions. Genetic counseling may also be recommended to discuss the implications of the test results and provide information on the inheritance pattern of the condition.

SKU: TEST-2447 Category:

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