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BAAT Gene Hypercholanemia Genetic Test Cost

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

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The BAAT Gene Hypercholanemia Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, aimed at identifying mutations in the BAAT gene, which are linked to hypercholanemia—a condition characterized by an abnormal increase in bile acid levels in the blood. This condition can lead to various gastrointestinal issues and liver diseases. By analyzing a patient’s DNA, the test can determine the presence of genetic alterations in the BAAT gene, providing essential information for the diagnosis, management, and treatment planning of hypercholanemia. The test is priced at 4400 AED, making it an accessible option for individuals in the UAE seeking comprehensive genetic analysis for this specific condition.

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BAAT Gene Hypercholanemia Genetic Test

At DNA Labs UAE, we offer the BAAT Gene Hypercholanemia Genetic Test to diagnose and analyze the symptoms of hypercholanemia. This test is designed to identify mutations in the BAAT gene that may be causing the condition.

Test Details

The BAAT gene, also known as bile acid-CoA:amino acid N-acyltransferase, plays a crucial role in the metabolism of bile acids in the liver. Mutations in this gene can lead to hypercholanemia, which is characterized by elevated levels of bile acids in the blood.

Our BAAT Gene Hypercholanemia Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. This advanced sequencing technology allows for a comprehensive analysis of the BAAT gene, aiding in the accurate diagnosis of hypercholanemia.

Test Components and Price

The cost of the BAAT Gene Hypercholanemia Genetic Test is 4400.0 AED. The test requires a blood sample, extracted DNA, or just one drop of blood on an FTA Card. The report will be delivered within 3 to 4 weeks.

Test Type and Doctor

The BAAT Gene Hypercholanemia Genetic Test falls under the category of Metabolic Disorders. It is recommended to consult a General Physician who specializes in genetics for this test.

Test Department and Pre Test Information

The BAAT Gene Hypercholanemia Genetic Test is conducted in our Genetics department. Before undergoing the test, it is essential 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 Hypercholanemia. This information helps in understanding the genetic background and inheritance patterns of the condition.

Importance and Benefits of the Test

NGS genetic testing for BAAT gene mutations plays a crucial role in the diagnosis and management of hypercholanemia. It provides valuable information for treatment, genetic counseling, and family planning purposes. By identifying the specific mutations in the BAAT gene, healthcare professionals can offer appropriate guidance and support to patients and their families.

It’s important to note that genetic testing should be ordered and interpreted by healthcare professionals with expertise in genetics, such as genetic counselors or medical geneticists. They possess the knowledge and experience to accurately interpret the test results and provide personalized recommendations.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to schedule your BAAT Gene Hypercholanemia Genetic Test and take a step towards better understanding and managing your health.

Test Name BAAT Gene Hypercholanemia 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 BAAT Gene Hypercholanemia NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypercholanemia
Test Details

The BAAT gene, also known as bile acid-CoA:amino acid N-acyltransferase, is involved in the metabolism of bile acids in the liver. Mutations in this gene can lead to a condition called hypercholanemia, which is characterized by elevated levels of bile acids in the blood.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of hypercholanemia, NGS genetic testing can be used to identify mutations in the BAAT gene that may be causing the condition.

NGS genetic testing for BAAT gene mutations can help with the diagnosis of hypercholanemia and provide valuable information for treatment and management of the condition. It can also be used for genetic counseling and family planning purposes.

It’s important to note that genetic testing should be ordered and interpreted by healthcare professionals with expertise in genetics, such as genetic counselors or medical geneticists. They can provide appropriate guidance and support based on the test results.

SKU: TEST-2427