NR1H4 Gene Cholestasis Infantile NR1H4 Related Genetic Test
At DNA Labs UAE, we offer the NR1H4 Gene Cholestasis Infantile NR1H4 Related Genetic Test for individuals suspected of having this rare genetic disorder. Cholestasis, infantile, NR1H4 related affects the liver and bile ducts and is caused by mutations in the NR1H4 gene.
Test Components and Price
The NR1H4 Gene Cholestasis Infantile NR1H4 Related Genetic Test is priced at 4400.0 AED. The test requires a sample of either blood, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Test Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test utilizes Next-Generation Sequencing (NGS) technology, which allows for the simultaneous analysis of multiple genes, including the NR1H4 gene.
Test Type and Doctor
The NR1H4 Gene Cholestasis Infantile NR1H4 Related Genetic Test falls under the categories of Hepatology, Nephrology, and Endocrinology Disorders. It is recommended to consult with a General Physician who specializes in genetics.
Test Department and Pre-Test Information
The test is conducted by our Genetics department. Before undergoing the NR1H4 Gene Cholestasis Infantile NR1H4 Related 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 NR1H4 Gene Cholestasis, infantile, NR1H4 related NGS Genetic DNA Test gene NR1H4.
Test Details and Diagnosis
Cholestasis, infantile, NR1H4 related is a rare genetic disorder that affects the liver and bile ducts. The NR1H4 gene is responsible for regulating the production and flow of bile acids in the liver. To diagnose cholestasis, infantile, NR1H4 related, the NR1H4 Gene Cholestasis Infantile NR1H4 Related Genetic Test can be performed.
The NGS technology used in this test involves extracting a small sample of DNA from the patient’s blood or saliva. This DNA is then sequenced, generating millions of short DNA sequences. These sequences are aligned with a reference genome, allowing for the identification of any variations or mutations in the NR1H4 gene.
If mutations are found in the NR1H4 gene, it confirms the diagnosis of cholestasis, infantile, NR1H4 related. This information can be crucial in guiding treatment decisions and providing important information for genetic counseling.
It is important to note that genetic testing for cholestasis, infantile, NR1H4 related should be performed by a qualified geneticist or genetic counselor. They possess the expertise to provide appropriate counseling and interpretation of the test results.
| Test Name | NR1H4 Gene Cholestasis infantile 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 Cholestasis, infantile, NR1H4 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NR1H4 Gene Cholestasis, infantile, NR1H4 related NGS Genetic DNA Test gene NR1H4 |
| Test Details |
Cholestasis, infantile, NR1H4 related is a rare genetic disorder that affects the liver and bile ducts. It is caused by mutations in the NR1H4 gene, which is responsible for regulating the production and flow of bile acids in the liver. To diagnose cholestasis, infantile, NR1H4 related, a Next-Generation Sequencing (NGS) genetic test can be performed. NGS is a high-throughput sequencing method that allows for the simultaneous analysis of multiple genes, including the NR1H4 gene. During the NGS test, a small sample of DNA is extracted from the patient’s blood or saliva. This DNA is then sequenced using NGS technology, which generates millions of short DNA sequences. These sequences are aligned with a reference genome, and any variations or mutations in the NR1H4 gene are identified. If mutations are found in the NR1H4 gene, it confirms the diagnosis of cholestasis, infantile, NR1H4 related. This information can help guide treatment decisions and provide important information for genetic counseling. It is important to note that genetic testing for cholestasis, infantile, NR1H4 related should be performed by a qualified geneticist or genetic counselor, as they can provide appropriate counseling and interpretation of the results. |
