SNRPN Gene Prader-Willi syndrome Genetic Test
At DNA Labs UAE, we offer the SNRPN Gene Prader-Willi syndrome Genetic Test. This test is designed to detect and diagnose Prader-Willi syndrome (PWS), a rare genetic disorder that affects various aspects of development and metabolism.
Test Details
The SNRPN gene is associated with PWS, which is caused by the loss of function of specific genes on chromosome 15. Our genetic test uses Next-Generation Sequencing (NGS) technology to analyze multiple genes simultaneously, including the SNRPN gene. This allows for a comprehensive and rapid analysis of genetic variations, such as deletions or mutations, associated with PWS.
Test Components and Price
The cost of the SNRPN Gene Prader-Willi syndrome Genetic Test is 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 Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test is conducted using NGS technology, which ensures accurate and efficient results.
Test Type and Doctor
The SNRPN Gene Prader-Willi syndrome Genetic Test falls under the category of Neurological Disorders. It is recommended to consult with a Neurologist for this test.
Test Department
The test is conducted in our Genetics department, where our skilled professionals ensure accurate and reliable results.
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient who is undergoing the SNRPN Gene Prader-Willi syndrome NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by SNRPN Gene Prader-Willi syndrome.
Benefits of the Test
Genetic testing for PWS using NGS technology can provide valuable information for individuals and families affected by the syndrome. It can help in the diagnosis of suspected cases, confirmation of a clinical diagnosis, identification of carriers of the genetic mutation, and prenatal testing in families with a known genetic mutation. The results of the test can also offer guidance for medical management, reproductive planning, and genetic counseling.
Consultation
It is crucial to consult with a healthcare professional or genetic counselor to fully understand the implications and limitations of the test results.
| Test Name | SNRPN Gene Prader-Willi syndrome Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for SNRPN Gene Prader-Willi syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SNRPN Gene Prader-Willi syndrome |
| Test Details |
The SNRPN gene is associated with Prader-Willi syndrome (PWS), a rare genetic disorder that affects many aspects of development and metabolism. PWS is caused by the loss of function of specific genes on chromosome 15, including the SNRPN gene. NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the rapid and comprehensive analysis of multiple genes simultaneously. It can be used to identify genetic variations, such as deletions or mutations, in the SNRPN gene and other genes associated with PWS. A genetic test using NGS for PWS can help diagnose individuals suspected of having the syndrome, confirm a clinical diagnosis, and identify carriers of the genetic mutation. It can also be used for prenatal testing in families with a known genetic mutation. The test typically involves collecting a DNA sample, usually through a blood sample or cheek swab, and sequencing the DNA using NGS technology. The results are then analyzed to determine if any genetic variations or mutations are present in the SNRPN gene or other relevant genes. Genetic testing for PWS can provide valuable information for individuals and families affected by the syndrome, including guidance for medical management, reproductive planning, and genetic counseling. It is important to consult with a healthcare professional or genetic counselor to understand the implications and limitations of the test results. |
