ASL Gene Argininosuccinic aciduria Genetic Test sale cost 4400 AED
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ASL Gene Argininosuccinic aciduria Genetic Test Cost

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

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The ASL Gene Argininosuccinic Aciduria Genetic Test is a specialized diagnostic procedure designed to detect mutations in the ASL gene, which is responsible for argininosuccinic aciduria (ASA). Argininosuccinic aciduria is a rare, inherited disorder that disrupts the urea cycle, a series of biochemical processes in the liver that help remove ammonia from the bloodstream. Individuals with this condition have difficulty breaking down ammonia, leading to its accumulation in the body, which can cause serious health problems, including brain damage, if not treated promptly.

This genetic test is crucial for early diagnosis and management of the condition. By analyzing a patient’s DNA, the test can identify specific mutations in the ASL gene that cause argininosuccinic aciduria, providing valuable information for treatment planning and genetic counseling.

The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the ASL Gene Argininosuccinic Aciduria Genetic Test is 4400 AED. This investment can be invaluable for affected families, offering them a clearer understanding of their genetic status and guiding them towards appropriate medical interventions to manage the condition effectively.

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ASL Gene Argininosuccinic aciduria Genetic Test

Components: ASL Gene Argininosuccinic aciduria Genetic Test

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

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 ASL Gene Argininosuccinic aciduria NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Argininosuccinic aciduria.

Test Details

The ASL Gene Argininosuccinic aciduria NGS Genetic Test is a type of genetic test that focuses on the ASL gene, which is responsible for the production of the enzyme argininosuccinate lyase (ASL). This test specifically looks for mutations or variations in the ASL gene that are associated with a condition called argininosuccinic aciduria (ASA).

Argininosuccinic aciduria is a rare genetic disorder that affects the urea cycle, which is responsible for removing ammonia from the body. Individuals with this condition are unable to break down argininosuccinic acid, leading to a buildup of ammonia in the blood. This can cause serious health problems, including intellectual disability, liver damage, and seizures.

The NGS (Next-Generation Sequencing) technique is used in this genetic test to analyze the DNA sequence of the ASL gene. NGS allows for the rapid and accurate sequencing of large portions of the genome, making it a valuable tool in genetic testing. By identifying mutations or variations in the ASL gene, this test can provide a diagnosis for individuals suspected of having argininosuccinic aciduria.

Overall, the ASL Gene Argininosuccinic aciduria NGS Genetic Test is an important tool in diagnosing and managing this rare genetic disorder. It can help healthcare professionals provide appropriate treatment and support for individuals with argininosuccinic aciduria.

Test Name ASL Gene Argininosuccinic aciduria Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
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 ASL Gene Argininosuccinic aciduria NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Argininosuccinic aciduria
Test Details

ASL Gene Argininosuccinic aciduria NGS Genetic Test is a type of genetic test that focuses on the ASL gene, which is responsible for the production of the enzyme argininosuccinate lyase (ASL). This test specifically looks for mutations or variations in the ASL gene that are associated with a condition called argininosuccinic aciduria (ASA).

Argininosuccinic aciduria is a rare genetic disorder that affects the urea cycle, which is responsible for removing ammonia from the body. Individuals with this condition are unable to break down argininosuccinic acid, leading to a buildup of ammonia in the blood. This can cause serious health problems, including intellectual disability, liver damage, and seizures.

The NGS (Next-Generation Sequencing) technique is used in this genetic test to analyze the DNA sequence of the ASL gene. NGS allows for the rapid and accurate sequencing of large portions of the genome, making it a valuable tool in genetic testing. By identifying mutations or variations in the ASL gene, this test can provide a diagnosis for individuals suspected of having argininosuccinic aciduria.

Overall, the ASL Gene Argininosuccinic aciduria NGS Genetic Test is an important tool in diagnosing and managing this rare genetic disorder. It can help healthcare professionals provide appropriate treatment and support for individuals with argininosuccinic aciduria.

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