TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome Genetic Test
Genetic testing plays a crucial role in diagnosing and understanding rare genetic disorders. One such disorder is Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT), which is associated with the TSPYL1 gene. This syndrome is characterized by the sudden death of male infants within the first year of life, along with underdeveloped or absent testes.
Test Details
The TSPYL1 gene can be analyzed using Next-Generation Sequencing (NGS) technology. This genetic testing method helps identify any mutations or variations in the TSPYL1 gene that may be present. By confirming a diagnosis of SIDDT, this test provides important information for families.
Test Components and Price
The TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome Genetic Test costs AED 4400.0. The sample condition required for this test includes blood, extracted DNA, or one drop of blood on an FTA Card. The report delivery time is estimated to be 3 to 4 weeks.
Test Type and Doctor
This genetic test falls under the category of Cardiovascular Pneumology Disorders. It is recommended to consult with a Cardiologist for this test.
Test Department and Pre Test Information
The TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome Genetic Test is conducted in the Genetics department. It is essential to provide the clinical history of the patient before undergoing this test. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by SIDDT.
Benefits of Genetic Testing for SIDDT
Genetic testing for SIDDT offers several benefits. Firstly, it helps understand the cause of the syndrome and provides insights into the likelihood of recurrence in future pregnancies. This information is crucial for families planning to have children. Secondly, genetic testing can guide medical management and provide appropriate genetic counseling for affected individuals and their families.
Overall, the TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome Genetic Test is an important tool for diagnosing and managing SIDDT. It offers valuable information for families affected by this rare genetic disorder.
| Test Name | TSPYL1 Gene Sudden infant death with dysgenesis of the testes 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 | Cardiovascular Pneumology Disorders |
| Doctor | Cardiologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for TSPYL1 Gene Sudden infant death with dysgenesis of the testes syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TSPYL1 Gene Sudden infant death with dysgenesis of the testes syndrome NGS Genetic DNA Test gene TSPYL1 |
| Test Details | The TSPYL1 gene is associated with a rare genetic disorder called Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT). This syndrome is characterized by the sudden death of male infants within the first year of life, as well as underdeveloped or absent testes. NGS (Next-Generation Sequencing) is a genetic testing method that can be used to analyze the TSPYL1 gene and identify any mutations or variations that may be present. This test can help confirm a diagnosis of SIDDT in individuals suspected to have the condition. Genetic testing for SIDDT can provide important information for families, including understanding the cause of the syndrome and the likelihood of recurrence in future pregnancies. It can also help guide medical management and provide genetic counseling for affected individuals and their families. |
