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ACADSB Gene 2-Methylbutyrylglycinuria Genetic Test Cost

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

-21%

The ACADSB gene 2-Methylbutyrylglycinuria genetic test is a specialized diagnostic procedure aimed at identifying mutations in the ACADSB gene, which are linked to the rare metabolic disorder known as 2-Methylbutyrylglycinuria. This condition affects the body’s ability to break down certain amino acids, leading to a buildup of specific substances that can be harmful. Symptoms of the disorder can vary and may include developmental delay, seizures, and metabolic crises, making early detection and management crucial for affected individuals.

The test involves analyzing the patient’s DNA to detect mutations in the ACADSB gene, which provides instructions for making an enzyme necessary for the breakdown of the amino acid isoleucine. A mutation in this gene can disrupt this process, leading to the accumulation of toxic substances in the body.

Conducted at DNA Labs UAE, a leading facility in genetic testing, the test is priced at 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in the field of genetic diagnostics, ensuring accurate and reliable test results. This genetic test is crucial for families with a history of 2-Methylbutyrylglycinuria, as it can provide essential information for the management of the condition, including dietary restrictions and monitoring for potential complications.

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ACADSB Gene 2-methylbutyrylglycinuria Genetic Test

Are you experiencing symptoms related to 2-methylbutyrylglycinuria? DNA Labs UAE offers the ACADSB Gene 2-methylbutyrylglycinuria Genetic Test at a cost of AED 4400.0. This test can help diagnose and manage the condition.

Test Details

The ACADSB gene is responsible for producing an enzyme called 2-methylbutyryl-CoA dehydrogenase, which is involved in breaking down certain amino acids in the body. Mutations in the ACADSB gene can lead to a condition called 2-methylbutyrylglycinuria, which is characterized by the inability to properly metabolize a specific amino acid called isoleucine.

To diagnose 2-methylbutyrylglycinuria, a genetic test can be performed using next-generation sequencing (NGS) technology. This test analyzes the DNA of an individual to identify any mutations or variations in the ACADSB gene that may be causing the condition. NGS genetic testing is a highly advanced and accurate method that allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of an individual’s genetic makeup.

Genetic testing can be particularly useful in cases where the symptoms of a genetic disorder are not clear or when there is a family history of the condition. It can also help determine the risk of passing on the condition to future generations and guide treatment decisions.

Test Components and Price

  • Test Name: ACADSB Gene 2-methylbutyrylglycinuria Genetic Test
  • Price: AED 4400.0
  • 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

Before undergoing the ACADSB Gene 2-methylbutyrylglycinuria 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 2-methylbutyrylglycinuria.

Consulting with a healthcare professional or genetic counselor is essential to understand the benefits, limitations, and implications of the test results.

Don’t let uncertainty linger. Take control of your health and get tested for 2-methylbutyrylglycinuria today at DNA Labs UAE!

Test Name ACADSB Gene 2-methylbutyrylglycinuria 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 ACADSB Gene 2-methylbutyrylglycinuria NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with 2-methylbutyrylglycinuria
Test Details

The ACADSB gene is responsible for producing an enzyme called 2-methylbutyryl-CoA dehydrogenase, which is involved in breaking down certain amino acids in the body. Mutations in the ACADSB gene can lead to a condition called 2-methylbutyrylglycinuria, which is characterized by the inability to properly metabolize a specific amino acid called isoleucine.

To diagnose 2-methylbutyrylglycinuria, a genetic test can be performed using next-generation sequencing (NGS) technology. This test analyzes the DNA of an individual to identify any mutations or variations in the ACADSB gene that may be causing the condition.

NGS genetic testing is a highly advanced and accurate method that allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of an individual’s genetic makeup. It can help identify the specific genetic variant(s) responsible for 2-methylbutyrylglycinuria, aiding in the diagnosis and management of the condition.

Genetic testing can be particularly useful in cases where the symptoms of a genetic disorder are not clear or when there is a family history of the condition. It can also help determine the risk of passing on the condition to future generations and guide treatment decisions.

It is important to consult with a healthcare professional or genetic counselor before undergoing any genetic testing to understand the benefits, limitations, and implications of the test results.

SKU: TEST-2128 Category:

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