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ABHD1 Gene Lung Alpha-beta Hydrolase Deficiency Type 1 Genetic Test

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

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The “ABHD1 Gene Lung Alpha-beta Hydrolase Deficiency Type 1 Genetic Test” is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at identifying mutations in the ABHD1 gene. This gene plays a critical role in the proper functioning of the lungs, and mutations can lead to Alpha-beta Hydrolase Deficiency Type 1, a rare genetic condition that affects lung function. The test is crucial for individuals who exhibit symptoms or have a family history of this condition, as it aids in the accurate diagnosis and subsequent management of the disorder.

Performed in the state-of-the-art facilities of DNA Labs UAE, the test involves analyzing the patient’s DNA to detect any abnormalities in the ABHD1 gene. The procedure is known for its precision and reliability, making it a valuable tool in the genetic evaluation of lung health.

The cost of the ABHD1 Gene Lung Alpha-beta Hydrolase Deficiency Type 1 Genetic Test is set at 4400 AED. While the price may seem high, it reflects the specialized nature of the test and the significant impact its results can have on a patient’s treatment plan and quality of life. Individuals undergoing this test at DNA Labs UAE can expect comprehensive support and guidance throughout the testing process, ensuring a smooth and informative experience.

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ABHD1 Gene Lung alpha-beta hydrolase deficiency type 1 Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing provider. Today, we will be discussing the ABHD1 Gene Lung alpha-beta hydrolase deficiency type 1 Genetic Test and its associated details.

Test Name: ABHD1 Gene Lung alpha-beta hydrolase deficiency type 1 Genetic Test

  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the ABHD1 Gene Lung alpha-beta hydrolase deficiency type 1 Genetic 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 Lung alpha-beta hydrolase deficiency type 1. This information will aid in the accurate diagnosis of the condition.

Test Details

The ABHD1 gene is responsible for producing an enzyme called alpha-beta hydrolase domain-containing protein 1. Mutations in this gene can lead to a condition known as lung alpha-beta hydrolase deficiency type 1. To diagnose this condition, a genetic test called Next-Generation Sequencing (NGS) can be performed.

NGS is a high-throughput method that allows for the simultaneous analysis of multiple genes, including the ABHD1 gene. This test involves sequencing the DNA of an individual to identify any mutations or variations in the ABHD1 gene that may be causing the deficiency.

The NGS genetic test can help confirm a diagnosis of lung alpha-beta hydrolase deficiency type 1 and provide valuable information about the specific genetic mutation involved. This information can be useful for understanding the underlying cause of the condition, predicting disease progression, and potentially guiding treatment decisions.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our team of experts, including general physicians and geneticists, are dedicated to assisting you throughout the testing process. If you have any questions or concerns, please do not hesitate to contact us.

Test Name ABHD1 Gene Lung alpha-beta hydrolase deficiency type 1 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 ABHD1 Gene Lung alpha-beta hydrolase deficiency type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Lung alpha-beta hydrolase deficiency type 1
Test Details

The ABHD1 gene is responsible for producing an enzyme called alpha-beta hydrolase domain-containing protein 1. Mutations in this gene can lead to a condition known as lung alpha-beta hydrolase deficiency type 1.

To diagnose this condition, a genetic test called Next-Generation Sequencing (NGS) can be performed. NGS is a high-throughput method that allows for the simultaneous analysis of multiple genes, including the ABHD1 gene. This test involves sequencing the DNA of an individual to identify any mutations or variations in the ABHD1 gene that may be causing the deficiency.

The NGS genetic test can help confirm a diagnosis of lung alpha-beta hydrolase deficiency type 1 and provide valuable information about the specific genetic mutation involved. This information can be useful for understanding the underlying cause of the condition, predicting disease progression, and potentially guiding treatment decisions.

SKU: TEST-2504 Category:

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