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ETFB Gene Acyl-CoA Multiple Dehydrogenase Deficiency Genetic Test

4,400 د.إ

-21%

The ETFB Gene Acyl-CoA Multiple Dehydrogenase Deficiency (MADD) Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the ETFB gene, which are implicated in the development of Multiple Acyl-CoA Dehydrogenase Deficiency (MADD). MADD, also known as Glutaric Acidemia Type II, is a rare metabolic disorder that disrupts the body’s ability to break down certain fats and proteins, leading to a variety of symptoms ranging from mild to severe, including metabolic crises.

This genetic test involves the analysis of the patient’s DNA to identify any abnormalities or mutations in the ETFB gene that could lead to the condition. The process is non-invasive, requiring only a blood sample from the patient. With a test cost of 4400 AED, it represents a critical step for individuals with a suspected diagnosis of MADD, enabling them to receive accurate diagnosis and appropriate management or treatment plans based on their genetic makeup.

DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in the field of genetic testing, ensuring high accuracy and reliability of test results. By opting for the ETFB Gene Acyl-CoA Multiple Dehydrogenase Deficiency Genetic Test, patients and their families can gain valuable insights into their genetic health, paving the way for personalized medical care and interventions to manage or mitigate the effects of MADD.

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ETFB Gene Acyl-CoA multiple dehydrogenase deficiency Genetic Test

At DNA Labs UAE, we offer the ETFB Gene Acyl-CoA multiple dehydrogenase deficiency Genetic Test at a cost of AED 4400.0. This test is designed to diagnose and identify mutations in the ETFB gene, which is responsible for the metabolism of fatty acids, amino acids, and choline.

Test Components

The test includes:

  • NGS Technology

Sample Condition

We accept blood or extracted DNA samples for this test. Alternatively, you can provide one drop of blood on an FTA card.

Report Delivery

You can expect to receive your test results within 3 to 4 weeks.

Test Type

This test falls under the category of Metabolic Disorders.

Referring Doctor

Your referring doctor for this test will be a General Physician.

Test Department

This test is conducted by our Genetics department.

Pre Test Information

Before undergoing the ETFB Gene Acyl-CoA multiple dehydrogenase deficiency Genetic Test, it is recommended to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by Acyl-CoA multiple dehydrogenase deficiency.

Test Details

ETFB Gene Acyl-CoA multiple dehydrogenase deficiency (ETFB-ACAD) is a rare genetic disorder that affects the metabolism of fatty acids, amino acids, and choline. This condition is caused by mutations in the ETFB gene, which encodes a protein involved in the electron transfer pathway.

NGS genetic testing, also known as Next-Generation Sequencing, is a cutting-edge technology used to analyze multiple genes simultaneously. In the case of ETFB-ACAD, NGS genetic testing can accurately identify mutations in the ETFB gene, enabling an accurate diagnosis of the condition.

During NGS genetic testing, DNA is extracted from a blood or saliva sample. The DNA is then sequenced using high-throughput methods, and the sequencing data is analyzed to identify any mutations or variants in the ETFB gene. This information is crucial for confirming a diagnosis of ETFB-ACAD and providing valuable insights for the treatment and management of the condition.

It is highly recommended to consult with a genetic counselor or healthcare professional before undergoing NGS genetic testing. This will help you understand the benefits, limitations, and potential implications of the test results.

Test Name ETFB Gene Acyl-CoA multiple dehydrogenase deficiency 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 ETFB Gene Acyl-CoA multiple dehydrogenase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Acyl-CoA multiple dehydrogenase deficiency
Test Details

ETFB Gene Acyl-CoA multiple dehydrogenase deficiency (ETFB-ACAD) is a rare genetic disorder that affects the metabolism of fatty acids, amino acids, and choline. It is caused by mutations in the ETFB gene, which encodes a protein involved in the electron transfer pathway.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of ETFB-ACAD, NGS genetic testing can be used to identify mutations in the ETFB gene, allowing for an accurate diagnosis of the condition.

NGS genetic testing involves extracting DNA from a blood or saliva sample, sequencing the DNA using high-throughput methods, and then analyzing the sequencing data to identify any mutations or variants in the ETFB gene. This can help confirm a diagnosis of ETFB-ACAD and provide valuable information for treatment and management of the condition.

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

SKU: TEST-2150 Category:

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