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AUH Gene 3-Methylglutaconic Aciduria Type 1 Genetic Test Cost

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

-21%

The AUH Gene 3-Methylglutaconic Aciduria Type 1 Genetic Test is a specialized diagnostic tool designed to detect mutations in the AUH gene, which are responsible for 3-Methylglutaconic Aciduria Type 1, a rare metabolic disorder. This condition is characterized by the body’s inability to properly process certain proteins, leading to an accumulation of 3-methylglutaconic acid and related compounds in the body. Symptoms can vary but may include developmental delay, intellectual disability, and other neurological or physical issues.

Performed at DNA Labs UAE, this genetic test involves analyzing the patient’s DNA to identify mutations in the AUH gene that indicate the presence of 3-Methylglutaconic Aciduria Type 1. The test is critical for early diagnosis, which can aid in managing symptoms and improving the quality of life for affected individuals.

The cost of the AUH Gene 3-Methylglutaconic Aciduria Type 1 Genetic Test is 4400 AED. This investment covers the sophisticated procedures required to accurately identify the genetic mutations associated with this condition. Given the complexity and the specialized nature of this test, it is conducted in the highly equipped and technologically advanced facilities of DNA Labs UAE, ensuring accurate and reliable results for patients and their families.

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  • This test is not intended for medical diagnosis or treatment
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AUH Gene 3-methylglutaconic aciduria type 1 Genetic Test

Cost: AED 4400.0

Symptoms and Diagnosis

3-methylglutaconic aciduria type 1 is a rare genetic disorder associated with the AUH gene. To diagnose this condition, a genetic test called AUH Gene 3-methylglutaconic aciduria type 1 Genetic Test is recommended. This test analyzes the DNA sequence of the AUH gene using NGS (Next Generation Sequencing) technology to identify any variations or mutations that may be causing the disorder.

Test Components

  • Price: AED 4400.0
  • 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 AUH Gene 3-methylglutaconic aciduria type 1 Genetic 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 3-methylglutaconic aciduria type 1.

Test Details

The AUH gene is associated with 3-methylglutaconic aciduria type 1, a rare genetic disorder. NGS genetic testing is a method used to analyze the DNA sequence of genes to identify any variations or mutations that may be causing a particular condition or disease. In the case of 3-methylglutaconic aciduria type 1, NGS genetic testing can be used to identify mutations in the AUH gene that are responsible for the condition. This type of testing can help with diagnosis, genetic counseling, and potential treatment options for individuals affected by this disorder.

Test Name AUH Gene 3-methylglutaconic aciduria type 1 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 AUH Gene 3-methylglutaconic aciduria type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with 3-methylglutaconic aciduria type 1
Test Details

The AUH gene is associated with 3-methylglutaconic aciduria type 1, a rare genetic disorder. NGS (Next Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes to identify any variations or mutations that may be causing a particular condition or disease. In the case of 3-methylglutaconic aciduria type 1, NGS genetic testing can be used to identify mutations in the AUH gene that are responsible for the condition. This type of testing can help with diagnosis, genetic counseling, and potential treatment options for individuals affected by this disorder.

SKU: TEST-2136 Category:

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