ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 Genetic Test sale cost 4400 AED
BLM Gene Bloom syndrome Genetic Test sale cost 4400 AED BLM Gene Bloom syndrome Genetic Test 5,600 د.إ 4,400 د.إ
SLC25A1 Gene Combined D-2- and L-2-hydroxyglutaric aciduria Genetic Test sale cost 3200 AED SLC25A1 Gene Combined D-2- and L-2-hydroxyglutaric aciduria Genetic Test 5,600 د.إ 3,200 د.إ
Sale!

ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 Genetic Test

4,400 د.إ

-21%

The ABCB11 gene plays a crucial role in the body by coding for the bile salt export pump (BSEP), which is essential for the transport of bile acids from liver cells into the bile ducts. Mutations in the ABCB11 gene can lead to a condition known as benign recurrent intraheptic cholestasis type 2 (BRIC2), characterized by episodes of liver dysfunction that can cause jaundice, itching, and elevated liver enzymes. These episodes are typically not associated with long-term liver damage and tend to recur throughout life.

To diagnose this condition, a genetic test targeting the ABCB11 gene can be performed. This test is particularly useful for individuals experiencing symptoms of cholestasis with no apparent cause, or for those with a family history of liver disorders. By analyzing the DNA for specific mutations in the ABCB11 gene, healthcare providers can confirm a diagnosis of BRIC2, which can significantly aid in the management and treatment of the condition.

In the UAE, DNA Labs UAE offers this specialized genetic test for the ABCB11 gene. The cost of the test is 4400 AED. This test is conducted in a state-of-the-art laboratory setting by professionals who specialize in genetic analysis. The results from this test can provide valuable information for the patient and their healthcare provider, enabling a tailored approach to treatment and management of the condition, as well as offering insights into the prognosis and potential need for monitoring of liver function over time.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 Genetic Test

At DNA Labs UAE, we offer the ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 Genetic Test for individuals who suspect they may have this genetic disorder affecting their liver. This test can provide valuable information about the condition, including symptoms, diagnosis, and the cost of the test.

Test Details

The ABCB11 gene is associated with Cholestasis benign recurrent intrahepatic type 2, a genetic disorder that causes episodes of cholestasis, which is a reduction or blockage of bile flow in the liver. Common symptoms of this condition include recurrent itching, jaundice (yellowing of the skin and eyes), and elevated levels of certain liver enzymes.

Our NGS (Next-Generation Sequencing) genetic testing method allows us to analyze multiple genes simultaneously to identify genetic variations or mutations that may be responsible for Cholestasis benign recurrent intrahepatic type 2. By identifying specific mutations or variations in the ABCB11 gene, this test can provide a definitive diagnosis for individuals with this condition.

NGS genetic testing is a comprehensive and accurate method that can provide valuable insights into an individual’s genetic makeup. It can guide treatment decisions and provide information about the risk of passing the condition on to future generations.

Test Components and Price

Test Name: ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 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 ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 Genetic Test, it is important 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 Cholestasis benign recurrent intrahepatic type 2. This information will help in accurately interpreting the test results.

At DNA Labs UAE, we prioritize providing accurate and reliable genetic testing services. Our team of experts is dedicated to assisting individuals in understanding their genetic makeup and providing appropriate guidance for their healthcare needs.

Test Name ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 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 ABCB11 Gene Cholestasis benign recurrent intrahepatic type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Cholestasis benign recurrent intrahepatic type 2
Test Details

The ABCB11 gene is associated with a condition called Cholestasis benign recurrent intrahepatic type 2. This is a genetic disorder that affects the liver and causes episodes of cholestasis, which is a reduction or blockage of bile flow. This condition is characterized by recurrent episodes of itching, jaundice (yellowing of the skin and eyes), and elevated levels of certain liver enzymes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously to identify genetic variations or mutations that may be responsible for a particular condition. In the case of Cholestasis benign recurrent intrahepatic type 2, NGS genetic testing can be used to identify mutations or variations in the ABCB11 gene that may be causing the condition.

By identifying the specific genetic mutation causing Cholestasis benign recurrent intrahepatic type 2, NGS genetic testing can provide a definitive diagnosis for individuals with this condition. This information can be useful for guiding treatment decisions and providing information about the risk of passing the condition on to future generations.

SKU: TEST-2217 Category:

Related products