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FLCN Gene Birt-Hogg-Dube Syndrome Genetic Test Cost

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

-21%

The FLCN Gene Birt-Hogg-Dubé Syndrome Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, aimed at identifying mutations in the FLCN gene, which are indicative of Birt-Hogg-Dubé (BHD) Syndrome. BHD Syndrome is a rare genetic condition characterized by skin lesions, lung cysts, and an increased risk of kidney tumors. The test plays a crucial role in the early detection and management of the syndrome, allowing for timely intervention and monitoring for associated complications.

This genetic test involves analyzing the patient’s DNA to look for specific mutations in the FLCN gene that are known to cause BHD Syndrome. It is usually recommended for individuals with a family history of the condition or those exhibiting symptoms related to BHD Syndrome.

The cost of the FLCN Gene Birt-Hogg-Dubé Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, covering the genetic analysis, professional interpretation of the results, and follow-up consultations to discuss the findings. Given the specialized nature of the test and its importance in the diagnosis and management of BHD Syndrome, the investment is considered valuable for those at risk of this genetic condition.

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FLCN Gene Birt-Hogg-Dube syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer the FLCN Gene Birt-Hogg-Dube syndrome Genetic Test. This test helps in diagnosing and managing Birt-Hogg-Dube syndrome, a rare genetic disorder characterized by the development of benign skin tumors, lung cysts, and an increased risk of kidney cancer.

Test Details

The FLCN gene is associated with Birt-Hogg-Dube syndrome (BHD). Our Next-Generation Sequencing (NGS) genetic testing method allows for the simultaneous analysis of multiple genes, including the FLCN gene, to identify potential mutations or variations.

NGS provides a comprehensive analysis of the entire gene sequence, enabling the detection of various types of genetic alterations. This includes point mutations, deletions, insertions, or duplications. By performing an NGS genetic test for the FLCN gene, our healthcare professionals can identify any mutations or variations present in an individual’s DNA.

Test Components and Price

  • Test Name: FLCN Gene Birt-Hogg-Dube 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to the FLCN Gene Birt-Hogg-Dube syndrome NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by the FLCN Gene Birt-Hogg-Dube syndrome NGS Genetic DNA Test gene FLCN.

Benefits of Genetic Testing

Genetic testing for Birt-Hogg-Dube syndrome can help in confirming a diagnosis, assessing the risk of developing associated symptoms, and guiding appropriate medical management and surveillance strategies. It is crucial to undergo genetic testing under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Contact us today to learn more about the FLCN Gene Birt-Hogg-Dube syndrome Genetic Test and how it can benefit you.

Test Name FLCN Gene Birt-Hogg-Dube 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 FLCN Gene Birt-Hogg-Dube syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FLCN Gene Birt-Hogg-Dube syndrome NGS Genetic DNA Test gene FLCN
Test Details

The FLCN gene is associated with Birt-Hogg-Dub syndrome (BHD), a rare genetic disorder characterized by the development of benign skin tumors (fibrofolliculomas), lung cysts, and an increased risk of kidney cancer.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the FLCN gene, to identify potential mutations or variations. NGS can provide a comprehensive analysis of the entire gene sequence, allowing for the detection of various types of genetic alterations, such as point mutations, deletions, insertions, or duplications.

By performing an NGS genetic test for the FLCN gene, healthcare professionals can identify any mutations or variations that may be present in an individual’s DNA. This information can help in confirming a diagnosis of Birt-Hogg-Dub syndrome, assessing the risk of developing associated symptoms, and guiding appropriate medical management and surveillance strategies.

It’s important to note that genetic testing for BHD and other genetic conditions should be conducted under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support.

SKU: TEST-4007 Category:

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