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LAS1L Gene Wilson-Turner syndrome Genetic Test Cost

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

-21%

The LAS1L Gene Wilson-Turner Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the LAS1L gene that are associated with Wilson-Turner Syndrome (WTS). Wilson-Turner Syndrome is a rare genetic disorder characterized by intellectual disability, obesity, gynecomastia, and hypogonadism. The condition is inherited in an X-linked recessive pattern, meaning it predominantly affects males.

This genetic test involves analyzing the patient’s DNA, extracted from a blood sample, to detect any abnormalities or mutations in the LAS1L gene that may indicate the presence of Wilson-Turner Syndrome. The process is aimed at individuals who exhibit symptoms of WTS or have a family history of the condition, offering them crucial insights into their genetic makeup and aiding in the accurate diagnosis of WTS.

The cost of the LAS1L Gene Wilson-Turner Syndrome Genetic Test at DNA Labs UAE is set at 4400 AED. This investment includes the collection of the sample, the genetic analysis, and a comprehensive report of the findings. The report not only provides a diagnosis but also offers valuable information that can guide the management and treatment of the condition, improving the quality of life for those affected by Wilson-Turner Syndrome.

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Genetic Lab Blog – LAS1L Gene Wilson-Turner Syndrome Genetic Test

Introduction

Wilson-Turner syndrome is a rare genetic disorder primarily affecting females. It is characterized by intellectual disability, developmental delay, and physical abnormalities. The LAS1L gene is associated with this syndrome.

Test Details

The LAS1L Gene Wilson-Turner Syndrome Genetic Test is a next-generation sequencing (NGS) genetic test. NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive analysis of an individual’s genetic makeup. This test specifically looks for mutations or variations in the LAS1L gene and other genes associated with Wilson-Turner syndrome.

Test Components and Price

Test Name: LAS1L Gene Wilson-Turner Syndrome Genetic Test

  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Hepatology Nephrology Endocrinology Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the LAS1L Gene Wilson-Turner Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to create a pedigree chart of family members affected by the syndrome and to discuss the implications of the test.

Importance of Genetic Testing

Genetic testing, including NGS testing, should always be performed by a qualified healthcare professional specializing in genetics. They can determine the appropriateness of genetic testing and provide counseling and support throughout the testing process.

Conclusion

The LAS1L Gene Wilson-Turner Syndrome Genetic Test is a valuable tool for diagnosing Wilson-Turner syndrome. It provides comprehensive genetic analysis and can identify any mutations or variations in the LAS1L gene or other genes associated with the syndrome. This information is crucial for guiding treatment and management options.

Test Name LAS1L Gene Wilson-Turner 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 Hepatology Nephrology Endocrinology Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LAS1L Gene Wilson-Turner syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LAS1L Gene Wilson-Turner syndrome NGS Genetic DNA Test gene LAS1L
Test Details

The LAS1L gene is associated with a rare genetic disorder called Wilson-Turner syndrome. Wilson-Turner syndrome is a genetic condition that primarily affects females. It is characterized by intellectual disability, developmental delay, and certain physical abnormalities.

Next-generation sequencing (NGS) genetic testing is a type of genetic test that can be used to analyze multiple genes simultaneously. This type of testing can provide a comprehensive analysis of an individual’s genetic makeup and identify any mutations or variations in the LAS1L gene or other genes associated with Wilson-Turner syndrome.

NGS genetic testing can help in the diagnosis of Wilson-Turner syndrome by identifying any genetic abnormalities that may be present in the LAS1L gene. It can also provide valuable information about the specific genetic changes that are causing the disorder, which can help guide treatment and management options.

It is important to note that genetic testing, including NGS testing, should be performed by a qualified healthcare professional who specializes in genetics. They can help determine if genetic testing is appropriate and provide counseling and support throughout the testing process.

SKU: TEST-3808 Category:

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