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TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The TSPYL1 Gene Sudden Infant Death with Dysgenesis of the Testes Syndrome (SIDDT) genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the TSPYL1 gene that are associated with SIDDT. This rare genetic disorder is characterized by sudden infant death, typically within the first year of life, along with abnormalities in the development of the testes. The test plays a crucial role in diagnosing affected individuals, providing essential information for family planning, and guiding clinical management.

Priced at 4400 AED, the test involves analyzing the individual’s DNA to detect specific mutations in the TSPYL1 gene that have been linked to the syndrome. The process requires a sample of the individual’s blood or saliva, which is then subjected to advanced genetic sequencing techniques to scrutinize the gene of interest.

By identifying the presence of mutations in the TSPYL1 gene, the test can confirm a diagnosis of SIDDT, enabling healthcare providers to offer appropriate counseling and support to affected families. It is a vital tool for understanding the genetic basis of the syndrome and can help in the development of targeted therapies in the future.

DNA Labs UAE is equipped with state-of-the-art facilities and employs highly skilled professionals to conduct this complex genetic testing, ensuring accurate and reliable results for those undergoing testing for SIDDT.

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  • This test is not intended for medical diagnosis or treatment
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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.

SKU: TEST-3479 Category:

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