CHRM3 Gene Prune Belly Syndrome Genetic Test
Welcome to DNA Labs UAE, a leading genetic testing laboratory in the UAE. In this blog post, we will discuss the CHRM3 Gene Prune Belly Syndrome Genetic Test, including its components, cost, symptoms, diagnosis, and more.
Test Name: CHRM3 Gene Prune Belly Syndrome Genetic Test
- Components: CHRM3 gene analysis
- 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
Before undergoing the CHRM3 Gene Prune Belly Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the condition.
Test Details
The CHRM3 gene is associated with Prune Belly Syndrome (PBS), also known as Eagle-Barrett syndrome. Prune Belly Syndrome is a rare genetic disorder characterized by the absence or severe underdevelopment of the abdominal muscles, urinary tract abnormalities, and undescended testicles in males.
NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the context of Prune Belly Syndrome, NGS genetic testing can be used to identify any mutations or variations in the CHRM3 gene that may be contributing to the development of the condition.
By analyzing the CHRM3 gene through NGS, healthcare professionals can determine if there are any specific genetic changes in this gene that may be associated with Prune Belly Syndrome. This information can be helpful in confirming a diagnosis, predicting the likelihood of passing on the condition to offspring, and guiding treatment decisions.
It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide accurate and personalized information about the implications of the results.
If you or a loved one is suspected to have Prune Belly Syndrome, consider undergoing the CHRM3 Gene Prune Belly Syndrome Genetic Test at DNA Labs UAE. Our experienced team of geneticists and counselors will guide you through the process and provide you with the necessary information for informed decision-making.
| Test Name | CHRM3 Gene Prune belly 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 CHRM3 Gene Prune belly syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CHRM3 Gene Prune belly syndrome NGS Genetic DNA Test gene CHRM3 |
| Test Details |
The CHRM3 gene is associated with Prune Belly Syndrome (PBS), also known as Eagle-Barrett syndrome. Prune Belly Syndrome is a rare genetic disorder characterized by the absence or severe underdevelopment of the abdominal muscles, urinary tract abnormalities, and undescended testicles in males. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, providing a comprehensive assessment of an individual’s genetic makeup. In the context of Prune Belly Syndrome, NGS genetic testing can be used to identify any mutations or variations in the CHRM3 gene that may be contributing to the development of the condition. By analyzing the CHRM3 gene through NGS, healthcare professionals can determine if there are any specific genetic changes in this gene that may be associated with Prune Belly Syndrome. This information can be helpful in confirming a diagnosis, predicting the likelihood of passing on the condition to offspring, and guiding treatment decisions. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide accurate and personalized information about the implications of the results. |
