PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome Genetic Test
At DNA Labs UAE, we offer the PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome Genetic Test for individuals suspected of having this rare genetic disorder. This test can help diagnose and provide valuable information about the syndrome.
Test Details
The PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome is a genetic disorder characterized by joint and skeletal abnormalities, as well as inflammation of the pericardium. It is caused by mutations in the PRG4 gene.
Test Components and Price
- Test Name: PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome 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: Dysmorphology
- Doctor: Pediatrics
- Test Department: Genetics
Pre Test Information
Before undergoing the PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome Genetic 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 by the syndrome. This helps in identifying potential genetic factors.
About NGS Technology
NGS (Next-Generation Sequencing) genetic testing is a cutting-edge technology that allows for the analysis of multiple genes simultaneously. This enables a more comprehensive analysis of the genetic material, making it particularly useful in diagnosing genetic disorders like the PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
Benefits of NGS Genetic Testing
- Confirms the diagnosis of PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Helps in cases where the clinical presentation is atypical or other diagnostic tests have been inconclusive
- Provides information about the specific genetic mutation causing the syndrome
- Useful for genetic counseling and family planning
Important Note
Genetic testing should always be done under the guidance of a healthcare professional with expertise in genetics. They can provide counseling and support throughout the testing process and help interpret the results in the context of the individual’s symptoms and medical history.
Test Name | PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome 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 PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome NGS Genetic DNA Test gene PRG4 |
Test Details |
PRG4 Gene Camptodactyly-arthropathy-coxa vara-pericarditis syndrome is a rare genetic disorder characterized by joint and skeletal abnormalities, as well as inflammation of the pericardium (the membrane surrounding the heart). It is caused by mutations in the PRG4 gene. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. This allows for a more comprehensive analysis of the genetic material and can help identify mutations in the PRG4 gene associated with Camptodactyly-arthropathy-coxa vara-pericarditis syndrome. NGS genetic testing can be helpful in confirming a diagnosis of this syndrome, especially in cases where the clinical presentation is atypical or when other diagnostic tests have been inconclusive. It can also provide information about the specific genetic mutation causing the syndrome, which can be useful for genetic counseling and family planning. It is important to note that genetic testing should be done under the guidance of a healthcare professional with expertise in genetics. They can provide counseling and support throughout the testing process and help interpret the results in the context of the individual’s symptoms and medical history. |