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ATP8B1 Gene Cholestasis intrahepatic of pregnancy type 1 Genetic Test Cost

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

-21%

The ATP8B1 gene plays a crucial role in maintaining proper liver function. Mutations in this gene can lead to a condition known as intrahepatic cholestasis of pregnancy type 1 (ICP1), a liver disorder that occurs during pregnancy. This condition can cause severe itching in the expectant mother and, in some cases, lead to complications for the baby.

To diagnose this genetic predisposition, DNA Labs UAE offers a specific genetic test targeting the ATP8B1 gene. This test is essential for women with a family history of ICP1 or those who have experienced symptoms related to this condition in previous pregnancies. Early detection through this genetic test can help in managing the symptoms more effectively and in making informed decisions regarding pregnancy.

The test cost is set at 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology used to identify mutations in the ATP8B1 gene accurately. By choosing to undergo this test at DNA Labs UAE, patients can expect reliable results backed by expert analysis, helping to ensure the well-being of both mother and child during pregnancy.

Description

ATP8B1 Gene Cholestasis Intrahepatic of Pregnancy Type 1 Genetic Test

Components: ATP8B1 Gene Cholestasis intrahepatic of pregnancy type 1 Genetic Test

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 ATP8B1 Gene Cholestasis, intrahepatic, of pregnancy, type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Cholestasis, intrahepatic, of pregnancy, type 1.

Test Details: ATP8B1 gene cholestasis, intrahepatic, of pregnancy, type 1 is a rare genetic disorder that affects the liver during pregnancy. It is characterized by the impaired flow of bile from the liver, leading to a buildup of bile acids in the liver and bloodstream.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify variations or mutations that may be associated with a particular condition. In the case of ATP8B1 gene cholestasis, intrahepatic, of pregnancy, type 1, NGS genetic testing can help identify mutations in the ATP8B1 gene that are responsible for the condition.

This type of genetic testing can be useful for diagnosing individuals with suspected ATP8B1 gene cholestasis, intrahepatic, of pregnancy, type 1, especially in cases where other diagnostic methods have been inconclusive. It can also be used for carrier testing in individuals who have a family history of the condition or for prenatal testing in families with a known ATP8B1 gene mutation.

By identifying the specific genetic mutation associated with ATP8B1 gene cholestasis, intrahepatic, of pregnancy, type 1, NGS genetic testing can help guide treatment decisions and provide valuable information for genetic counseling.

Test Name	ATP8B1 Gene Cholestasis intrahepatic of pregnancy 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 ATP8B1 Gene Cholestasis, intrahepatic, of pregnancy, type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Cholestasis, intrahepatic, of pregnancy, type 1
Test Details	ATP8B1 gene cholestasis, intrahepatic, of pregnancy, type 1 is a rare genetic disorder that affects the liver during pregnancy. It is characterized by the impaired flow of bile from the liver, leading to a buildup of bile acids in the liver and bloodstream. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify variations or mutations that may be associated with a particular condition. In the case of ATP8B1 gene cholestasis, intrahepatic, of pregnancy, type 1, NGS genetic testing can help identify mutations in the ATP8B1 gene that are responsible for the condition. This type of genetic testing can be useful for diagnosing individuals with suspected ATP8B1 gene cholestasis, intrahepatic, of pregnancy, type 1, especially in cases where other diagnostic methods have been inconclusive. It can also be used for carrier testing in individuals who have a family history of the condition or for prenatal testing in families with a known ATP8B1 gene mutation. By identifying the specific genetic mutation associated with ATP8B1 gene cholestasis, intrahepatic, of pregnancy, type 1, NGS genetic testing can help guide treatment decisions and provide valuable information for genetic counseling.