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PTEN Gene Cowden Syndrome Type 1 Genetic Test Cost

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

-21%

The PTEN Gene Cowden Syndrome Type 1 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the PTEN gene, which are associated with Cowden Syndrome Type 1. This condition is a rare, autosomal dominant disorder characterized by multiple noncancerous, tumor-like growths called hamartomas and an increased risk of developing certain types of cancer, including breast, thyroid, and endometrial cancer. Early detection through genetic testing can be crucial for affected individuals and their families, as it allows for the implementation of targeted surveillance and preventive measures to manage the associated risks. The test is priced at 4400 AED and provides a comprehensive analysis of the PTEN gene to help in the diagnosis and management of Cowden Syndrome Type 1, thereby offering a valuable resource for individuals with a family history or clinical symptoms suggestive of this genetic condition.

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PTEN Gene Cowden Syndrome Type 1 Genetic Test

At DNA Labs UAE, we offer the PTEN Gene Cowden Syndrome Type 1 Genetic Test for individuals who may be at risk of this rare genetic disorder. This test can help identify mutations or variations in the PTEN gene that may be responsible for the development of Cowden syndrome type 1.

Test Details

The PTEN gene is associated with Cowden syndrome type 1, a genetic disorder characterized by the development of multiple noncancerous tumors called hamartomas. These tumors can affect various organs and tissues in the body, including the skin, thyroid, breast, and gastrointestinal tract.

Our PTEN Gene Cowden Syndrome Type 1 Genetic Test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes. This advanced sequencing technique helps identify any mutations or variations in the PTEN gene that may be present.

Components and Price

  • Test Name: PTEN Gene Cowden Syndrome Type 1 Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: 4400.0 AED

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA card for this test.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Method

We utilize NGS technology for the PTEN Gene Cowden Syndrome Type 1 Genetic Test.

Test Type

This test focuses on the genetic analysis of cancer-related genes.

Doctor and Test Department

This test is conducted under the supervision of an Oncologist in our Genetics Test Department.

Pre Test Information

Prior to the test, we require the clinical history of the patient who is undergoing the PTEN Gene Cowden Syndrome Type 1 Genetic Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by this genetic disorder.

Test Availability

It’s important to note that NGS genetic testing for Cowden syndrome type 1 may not be readily available in all healthcare settings. It is typically performed by specialized genetic testing laboratories or centers that have the expertise and infrastructure to perform comprehensive genetic analyses.

Genetic counseling is often recommended before and after NGS testing to help individuals understand the implications of the test results and make informed decisions about their healthcare.

Test Name PTEN Gene Cowden syndrome type 1 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 Cancer
Doctor Oncologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PTEN Gene Cowden syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTEN Gene Cowden syndrome type 1 NGS Genetic DNA Test gene PTEN
Test Details

The PTEN gene is associated with Cowden syndrome type 1, which is a rare genetic disorder characterized by the development of multiple noncancerous tumors called hamartomas. These tumors can affect various organs and tissues in the body, including the skin, thyroid, breast, and gastrointestinal tract.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Cowden syndrome type 1, NGS genetic testing can be used to identify mutations or variations in the PTEN gene that may be responsible for the development of the condition.

NGS genetic testing for Cowden syndrome type 1 typically involves obtaining a blood or saliva sample from the individual undergoing testing. The DNA in the sample is then sequenced to identify any mutations or variations in the PTEN gene. This information can help confirm a diagnosis of Cowden syndrome type 1 and guide treatment and management strategies for affected individuals and their families.

It’s important to note that NGS genetic testing for Cowden syndrome type 1 may not be readily available in all healthcare settings. It is typically performed by specialized genetic testing laboratories or centers that have the expertise and infrastructure to perform comprehensive genetic analyses. Genetic counseling is often recommended before and after NGS testing to help individuals understand the implications of the test results and make informed decisions about their healthcare.

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