JAG1 Gene Alagille Syndrome Type 1 Genetic Test
Components: JAG1 Gene Alagille syndrome 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: Dysmorphology
Doctor: Pediatrics
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for JAG1 Gene Alagille syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with JAG1 Gene Alagille syndrome type 1 NGS Genetic DNA Test gene JAG1
Test Details
The JAG1 gene is associated with a genetic disorder called Alagille syndrome type 1. Alagille syndrome is a rare genetic disorder that affects multiple systems in the body, including the liver, heart, and other organs.
NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of Alagille syndrome type 1, NGS can be used to identify mutations or variations in the JAG1 gene that may be responsible for the disorder.
NGS genetic testing for Alagille syndrome type 1 involves obtaining a DNA sample, usually through a blood sample or cheek swab, and then sequencing the JAG1 gene to look for any genetic changes. These changes may include small mutations, deletions, or duplications in the gene that can disrupt its normal function.
By identifying specific genetic changes in the JAG1 gene, NGS testing can help confirm a diagnosis of Alagille syndrome type 1 in individuals with suspected symptoms. It can also be used for carrier testing in family members of affected individuals or for prenatal testing in pregnancies at risk for the disorder.
It is important to note that genetic testing, including NGS, should always be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate counseling and support.
| Test Name | JAG1 Gene Alagille syndrome 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 | Dysmorphology |
| Doctor | Pediatrics |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for JAG1 Gene Alagille syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with JAG1 Gene Alagille syndrome type 1 NGS Genetic DNA Test gene JAG1 |
| Test Details |
The JAG1 gene is associated with a genetic disorder called Alagille syndrome type 1. Alagille syndrome is a rare genetic disorder that affects multiple systems in the body, including the liver, heart, and other organs. NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of Alagille syndrome type 1, NGS can be used to identify mutations or variations in the JAG1 gene that may be responsible for the disorder. NGS genetic testing for Alagille syndrome type 1 involves obtaining a DNA sample, usually through a blood sample or cheek swab, and then sequencing the JAG1 gene to look for any genetic changes. These changes may include small mutations, deletions, or duplications in the gene that can disrupt its normal function. By identifying specific genetic changes in the JAG1 gene, NGS testing can help confirm a diagnosis of Alagille syndrome type 1 in individuals with suspected symptoms. It can also be used for carrier testing in family members of affected individuals or for prenatal testing in pregnancies at risk for the disorder. It is important to note that genetic testing, including NGS, should always be done under the guidance of a healthcare professional or genetic counselor who can help interpret the results and provide appropriate counseling and support. |
