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ETFA Gene Acyl-CoA Multiple Dehydrogenase Deficiency Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 3,200 د.إ.

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The “ETFA Gene Acyl-CoA Multiple Dehydrogenase Deficiency Genetic Test” is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the ETFA gene. These mutations are responsible for a condition known as Multiple Acyl-CoA Dehydrogenase Deficiency (MADD), also referred to as Glutaric Acidemia Type II. MADD is a metabolic disorder that affects the body’s ability to break down certain fats and proteins, leading to a range of symptoms from mild to severe, including metabolic crises.

The test specifically targets the ETFA gene, one of the genes involved in the electron transfer flavoprotein complex, crucial for the proper function of the mitochondrial respiratory chain. Mutations in this gene disrupt normal metabolism, leading to the accumulation of fatty acids and organic acids in the body, which can be toxic and lead to the symptoms associated with MADD.

DNA Labs UAE offers this genetic test at a cost of 3200 AED. The test is conducted through a simple blood sample, where DNA is extracted and analyzed for mutations in the ETFA gene. This genetic testing is crucial for early diagnosis, which can significantly improve the management and prognosis of the condition. Early intervention with dietary management and, in some cases, supplements or medications can help manage the symptoms and prevent metabolic crises.

Families with a history of MADD or individuals showing symptoms related to metabolic dysfunction may consider undergoing this genetic test. It is also a valuable tool for genetic counseling, helping at-risk couples understand their chances of having a child with the condition. DNA Labs UAE provides this test with professional guidance and support, ensuring that individuals and families receive comprehensive information about the condition and the implications of the test results.

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ETFA Gene Acyl-CoA multiple dehydrogenase deficiency Genetic Test

Are you concerned about Acyl-CoA multiple dehydrogenase deficiency? DNA Labs UAE offers the ETFA Gene Acyl-CoA multiple dehydrogenase deficiency Genetic Test to provide you with valuable insights into this rare genetic disorder.

Test Components

  • Price: 3200.0 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

Prior to undergoing the ETFA Gene Acyl-CoA multiple dehydrogenase deficiency NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with Acyl-CoA multiple dehydrogenase deficiency.

Test Details

ETFA Gene Acyl-CoA multiple dehydrogenase deficiency is a rare genetic disorder that affects the metabolism of fats and proteins. This disorder is caused by mutations in the ETFA gene, which provides instructions for making an enzyme called electron transfer flavoprotein alpha subunit. The enzyme is involved in the process of fatty acid oxidation, which breaks down fats and proteins for energy production.

The NGS Genetic Test, also known as Next-Generation Sequencing Genetic Test, is a cutting-edge genetic testing method that allows for the simultaneous analysis of multiple genes. By using advanced sequencing technologies, this test can detect mutations or variations in the DNA sequence associated with genetic disorders, including ETFA Gene Acyl-CoA multiple dehydrogenase deficiency.

The ETFA Gene Acyl-CoA multiple dehydrogenase deficiency NGS Genetic Test involves obtaining a DNA sample, usually through a blood sample or a cheek swab. The DNA is then sequenced using next-generation sequencing technology, which can rapidly and accurately analyze the entire coding region of the ETFA gene. The sequencing data is analyzed and compared to a reference sequence to identify any genetic variations or mutations.

The results of the NGS Genetic Test provide valuable information about the presence of mutations in the ETFA gene, confirming a diagnosis of Acyl-CoA multiple dehydrogenase deficiency. Additionally, the specific mutations identified can be useful for genetic counseling and family planning.

It is important to note that genetic testing, including the NGS Genetic Test, should be performed and interpreted by qualified healthcare professionals with expertise in genetics. These professionals can provide appropriate counseling and guidance based on the individual’s test results.

Test Name ETFA Gene Acyl-CoA multiple dehydrogenase deficiency Genetic Test
Components
Price 3200.0 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 ETFA 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

ETFA Gene Acyl-CoA multiple dehydrogenase deficiency is a rare genetic disorder that affects the metabolism of fats and proteins. It is caused by mutations in the ETFA gene, which provides instructions for making an enzyme called electron transfer flavoprotein alpha subunit. This enzyme is involved in a process called fatty acid oxidation, which breaks down fats and proteins for energy production.

NGS Genetic Test, also known as Next-Generation Sequencing Genetic Test, is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of mutations or variations in the DNA sequence that may be associated with genetic disorders, including ETFA Gene Acyl-CoA multiple dehydrogenase deficiency.

The NGS Genetic Test for ETFA Gene Acyl-CoA multiple dehydrogenase deficiency involves obtaining a DNA sample, usually through a blood sample or a cheek swab. The DNA is then sequenced using next-generation sequencing technology, which can rapidly and accurately analyze the entire coding region of the ETFA gene. The sequencing data is then analyzed and compared to a reference sequence to identify any genetic variations or mutations.

The results of the NGS Genetic Test can provide valuable information about the presence of mutations in the ETFA gene, which can help confirm a diagnosis of Acyl-CoA multiple dehydrogenase deficiency. It can also provide information about the specific mutations identified, which can be useful for genetic counseling and family planning.

It is important to note that genetic testing, including NGS Genetic Test, should be performed and interpreted by qualified healthcare professionals with expertise in genetics. They can provide appropriate counseling and guidance based on the individual’s test results.

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