NR1H4 Gene Intrahepatic Cholestasis of Pregnancy NR1H4 Related Genetic Test
Welcome to DNA Labs UAE, where we offer comprehensive genetic testing services. In this blog post, we will discuss the NR1H4 gene intrahepatic cholestasis of pregnancy NR1H4 related genetic test.
Test Details
The NR1H4 gene is associated with a condition called intrahepatic cholestasis of pregnancy (ICP). ICP is a liver disorder that occurs during pregnancy and is characterized by impaired bile flow, leading to a buildup of bile acids in the liver. This condition can cause itching, jaundice, and other complications for both the mother and the baby.
NGS genetic testing refers to Next-Generation Sequencing, which is a high-throughput method used to analyze multiple genes simultaneously. NR1H4-related NGS genetic testing specifically focuses on sequencing the NR1H4 gene to identify any genetic variations or mutations that may be associated with ICP.
By identifying genetic variations in the NR1H4 gene, healthcare providers can better understand the underlying causes of ICP and provide personalized treatment and management strategies for affected individuals. This type of genetic testing can also help with genetic counseling and family planning for individuals at risk of passing on the condition to their children.
Test Components and Price
- Test Name: NR1H4 Gene Intrahepatic Cholestasis of Pregnancy NR1H4 Related Genetic Test
- Components: NGS Technology
- Price: 4400.0 AED
- Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
- Report Delivery: 3 to 4 Weeks
- Test Type: Hepatology Nephrology Endocrinology Disorders
- Doctor: General Physician
- Test Department: Genetics
Pre Test Information
Before undergoing the NR1H4 gene intrahepatic cholestasis of pregnancy NR1H4 related NGS genetic DNA test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with NR1H4 gene intrahepatic cholestasis of pregnancy and NR1H4 related NGS genetic DNA test gene NR1H4.
This pre-test information helps healthcare providers better understand the patient’s medical background and familial genetic history, allowing for a more accurate interpretation of the test results.
Conclusion
The NR1H4 gene intrahepatic cholestasis of pregnancy NR1H4 related genetic test offered by DNA Labs UAE is a valuable tool in diagnosing and managing ICP. By identifying genetic variations in the NR1H4 gene, healthcare providers can provide personalized treatment plans and assist with genetic counseling and family planning.
If you suspect you or a loved one may be at risk for ICP, consider getting the NR1H4 gene intrahepatic cholestasis of pregnancy NR1H4 related genetic test. Contact DNA Labs UAE today to learn more about this test and how it can benefit you.
Test Name | NR1H4 Gene Intrahepatic cholestasis of pregnancy NR1H4 related 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 | Hepatology Nephrology Endocrinology Disorders |
Doctor | General Physician |
Test Department: | Genetics |
Pre Test Information | Clinical History of Patient who is going for NR1H4 Gene Intrahepatic cholestasis of pregnancy, NR1H4 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NR1H4 Gene Intrahepatic cholestasis of pregnancy, NR1H4 related NGS Genetic DNA Test gene NR1H4 |
Test Details |
The NR1H4 gene is associated with a condition called intrahepatic cholestasis of pregnancy (ICP). ICP is a liver disorder that occurs during pregnancy and is characterized by impaired bile flow, leading to a buildup of bile acids in the liver. This condition can cause itching, jaundice, and other complications for both the mother and the baby. NGS genetic testing refers to Next-Generation Sequencing, which is a high-throughput method used to analyze multiple genes simultaneously. NR1H4-related NGS genetic testing specifically focuses on sequencing the NR1H4 gene to identify any genetic variations or mutations that may be associated with ICP. By identifying genetic variations in the NR1H4 gene, healthcare providers can better understand the underlying causes of ICP and provide personalized treatment and management strategies for affected individuals. This type of genetic testing can also help with genetic counseling and family planning for individuals at risk of passing on the condition to their children. |