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DIS3L2 Gene Perlman Syndrome Genetic Test Cost

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

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Perlman Syndrome is a rare genetic disorder characterized by overgrowth, kidney abnormalities, and an increased risk of Wilms’ tumor in infancy and childhood. It is caused by mutations in the DIS3L2 gene. The DIS3L2 gene plays a crucial role in cellular RNA metabolism, and mutations in this gene lead to the abnormal development and function of various body systems.

To diagnose Perlman Syndrome, a specific genetic test targeting the DIS3L2 gene can be performed. This test involves analyzing the patient’s DNA to identify mutations in the DIS3L2 gene that are associated with the syndrome. The availability of such a test is a significant step forward in the early detection and management of Perlman Syndrome, allowing for timely intervention and monitoring for potential complications.

In the UAE, DNA Labs UAE offers this specialized genetic test for Perlman Syndrome. The test cost is set at 4400 AED, reflecting the intricate processes involved in genetic analysis and the specialized expertise required to interpret the results accurately. Undergoing this test at DNA Labs UAE ensures that individuals suspected of having Perlman Syndrome or those with a family history of the disorder can receive a definitive diagnosis. This, in turn, facilitates the implementation of appropriate management strategies and supportive care to improve the quality of life for affected individuals and their families.

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DIS3L2 Gene Perlman Syndrome Genetic Test

Introduction

The DIS3L2 Gene Perlman Syndrome Genetic Test is a specialized genetic test offered by DNA Labs UAE. This blog post provides detailed information about the test, including its components, cost, symptoms, diagnosis, and more.

Test Components and Price

The DIS3L2 Gene Perlman Syndrome Genetic Test is priced at 4400.0 AED. The test requires a sample condition of either blood, extracted DNA, or one drop of blood on an FTA Card.

Report Delivery and Method

The test results are delivered within 3 to 4 weeks. The method used for the test is NGS (Next-Generation Sequencing) Technology.

Test Type and Doctor

The DIS3L2 Gene Perlman Syndrome Genetic Test falls under the category of Dysmorphology. It is recommended to consult a Pediatrics doctor for this test.

Test Department

The test is conducted in the Genetics department of DNA Labs UAE.

Pre Test Information

Prior to undergoing the DIS3L2 Gene Perlman Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by DIS3L2 Gene Perlman Syndrome NGS Genetic DNA Test gene DIS3L2.

Test Details

The DIS3L2 gene Perlman syndrome NGS genetic test is a type of genetic test that analyzes the DIS3L2 gene for mutations associated with Perlman syndrome. Perlman syndrome is a rare genetic disorder characterized by kidney abnormalities, overgrowth, developmental delays, and an increased risk of Wilms tumor (a type of kidney cancer).

Next-generation sequencing (NGS) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of the DIS3L2 gene Perlman syndrome NGS genetic test, the test involves sequencing the entire coding region of the DIS3L2 gene to identify any mutations or variants associated with Perlman syndrome.

This genetic test can help confirm a diagnosis of Perlman syndrome in individuals with clinical symptoms and can also be used for carrier testing in individuals with a family history of the condition. Identifying the specific genetic mutation in an affected individual or carrier can provide important information for genetic counseling and family planning purposes.

Test Name DIS3L2 Gene Perlman 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 DIS3L2 Gene Perlman Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DIS3L2 Gene Perlman Syndrome NGS Genetic DNA Test gene DIS3L2
Test Details

DIS3L2 gene Perlman syndrome NGS genetic test is a type of genetic test that analyzes the DIS3L2 gene for mutations associated with Perlman syndrome. Perlman syndrome is a rare genetic disorder characterized by a variety of symptoms including kidney abnormalities, overgrowth, developmental delays, and an increased risk of Wilms tumor (a type of kidney cancer).

Next-generation sequencing (NGS) is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes or even the entire genome. In the case of the DIS3L2 gene Perlman syndrome NGS genetic test, the test would involve sequencing the entire coding region of the DIS3L2 gene to identify any mutations or variants that may be associated with Perlman syndrome.

This genetic test can help confirm a diagnosis of Perlman syndrome in individuals with clinical symptoms and can also be used for carrier testing in individuals with a family history of the condition. Identifying the specific genetic mutation in an affected individual or carrier can also provide important information for genetic counseling and family planning purposes.

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