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ABCC2 Gene Dubin-Johnson Syndrome Genetic Test Cost

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

-21%

The ABCC2 gene, associated with Dubin-Johnson Syndrome, is a critical focus for genetic testing at DNA Labs UAE. Dubin-Johnson Syndrome is a rare genetic disorder characterized by an increase of conjugated bilirubin without elevation of liver enzymes (ALT, AST). It’s a condition that affects the liver’s ability to process certain substances, leading to jaundice. This syndrome is inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the defective gene, one from each parent, to be affected.

The genetic test for Dubin-Johnson Syndrome at DNA Labs UAE specifically targets mutations in the ABCC2 gene, which encodes for a protein essential for the proper functioning of the liver. Mutations in this gene disrupt the liver’s ability to transport certain compounds, including bilirubin, leading to the symptoms associated with the syndrome.

The cost of the ABCC2 gene test for Dubin-Johnson Syndrome at DNA Labs UAE is 4400 AED. This comprehensive test is designed to provide accurate diagnosis, which is crucial for the management and treatment of the condition. Early diagnosis can help in managing symptoms effectively and in making informed decisions about the care and treatment of individuals with the syndrome.

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ABCC2 Gene Dubin-Johnson Syndrome Genetic Test

Cost: AED 4400.0

At DNA Labs UAE, we offer the ABCC2 Gene Dubin-Johnson Syndrome Genetic Test for AED 4400.0. This test helps diagnose Dubin-Johnson syndrome, a rare genetic disorder that affects the liver’s ability to process bilirubin.

Test Components

  • Price: AED 4400.0
  • Sample Condition: Blood
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Hepatology, Nephrology, Endocrinology Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Before undergoing the ABCC2 Gene Dubin-Johnson Syndrome 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 by the syndrome.

Test Details

The ABCC2 gene is associated with Dubin-Johnson syndrome. This rare genetic disorder impairs the liver’s ability to process bilirubin, resulting in its buildup and causing a yellowish discoloration of the skin and eyes known as jaundice.

NGS (Next-Generation Sequencing) genetic testing is used to analyze an individual’s DNA sequence and identify any variations or mutations in specific genes, including the ABCC2 gene. This test helps diagnose Dubin-Johnson syndrome by detecting abnormalities in the ABCC2 gene that may be causing the condition.

By identifying the specific genetic mutation responsible for Dubin-Johnson syndrome, NGS genetic testing provides valuable information for diagnosis, prognosis, and treatment planning. It also helps determine the risk of passing on the condition to future generations.

It is crucial to note that genetic testing should always be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

Test Name ABCC2 Gene Dubin-Johnson syndrome Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ABCC2 Gene Dubin-Johnson syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ABCC2 Gene Dubin-Johnson syndrome NGS Genetic DNA Test gene ABCC2
Test Details

The ABCC2 gene is associated with a condition called Dubin-Johnson syndrome. This syndrome is a rare genetic disorder that affects the liver’s ability to process bilirubin, a substance produced when red blood cells are broken down. As a result, bilirubin builds up in the liver and can cause a yellowish discoloration of the skin and eyes, known as jaundice.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze an individual’s DNA sequence and identify any variations or mutations in specific genes, including the ABCC2 gene. This test can help diagnose Dubin-Johnson syndrome by detecting any abnormalities in the ABCC2 gene that may be causing the condition.

By identifying the specific genetic mutation responsible for Dubin-Johnson syndrome, NGS genetic testing can provide valuable information for diagnosis, prognosis, and treatment planning. It can also help in determining the risk of passing on the condition to future generations.

It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate guidance and support.

SKU: TEST-3605 Category:

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