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FBLIM1 Gene Kindler Syndrome Genetic Test Cost

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

-21%

The FBLIM1 gene Kindler Syndrome genetic test is a specialized diagnostic examination offered by DNA Labs UAE to identify mutations in the FBLIM1 gene, which are associated with Kindler Syndrome. Kindler Syndrome is a rare genetic disorder characterized by skin fragility, blistering, and photosensitivity, among other symptoms. It is inherited in an autosomal recessive manner, meaning that an individual must inherit two altered copies of the FBLIM1 gene, one from each parent, to be affected by the condition.

The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect the presence of specific mutations in the FBLIM1 gene that are known to cause Kindler Syndrome. This genetic testing is crucial for confirming the diagnosis, understanding the risk of passing the condition to offspring, and guiding management and treatment options for affected individuals.

The cost of the FBLIM1 gene Kindler Syndrome genetic test at DNA Labs UAE is 4400 AED. This cost covers the full process of the genetic testing, from sample collection to the detailed analysis and reporting of the results. It is advisable for individuals who have a family history of Kindler Syndrome or who exhibit symptoms of the disorder to consider undergoing this test. Early diagnosis through genetic testing can significantly improve the quality of life for those affected by providing access to appropriate care and interventions.

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FBLIM1 Gene Kindler Syndrome Genetic Test

Welcome to DNA Labs UAE, where we offer advanced genetic testing services. In this blog post, we will discuss the FBLIM1 Gene Kindler Syndrome Genetic Test, including its components, cost, symptoms, diagnosis, and more.

Test Details

The FBLIM1 gene is associated with a rare genetic disorder called Kindler syndrome. Kindler syndrome is an autosomal recessive disorder characterized by skin fragility, blistering, and photosensitivity. It is caused by mutations in the FBLIM1 gene, which encodes a protein called filamin B interacting protein 1.

Test Components

The FBLIM1 Gene Kindler Syndrome Genetic Test includes:

  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Test Cost

The cost of the FBLIM1 Gene Kindler Syndrome Genetic Test is 4400.0 AED.

Symptoms and Diagnosis

Common symptoms of Kindler syndrome include skin fragility, blistering, and photosensitivity. If you suspect that you or a family member may have Kindler syndrome, it is important to consult with a dermatologist. A genetic counselling session may be conducted to draw a pedigree chart of family members affected with FBLIM1 Gene Kindler Syndrome Genetic Test gene FBLIM1.

NGS Technology

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of mutations or variations in the DNA sequence. In the context of Kindler syndrome, NGS genetic testing can be used to detect mutations in the FBLIM1 gene to confirm a diagnosis. This type of testing is particularly useful for rare genetic disorders like Kindler syndrome, as it allows for a comprehensive analysis of multiple genes at once.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. If you have any questions or would like to schedule an appointment for the FBLIM1 Gene Kindler Syndrome Genetic Test, please contact us.

Test Name FBLIM1 Gene Kindler 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FBLIM1 Gene Kindler syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FBLIM1 Gene Kindler syndrome NGS Genetic DNA Test gene FBLIM1
Test Details

The FBLIM1 gene is associated with a rare genetic disorder called Kindler syndrome. Kindler syndrome is an autosomal recessive disorder characterized by skin fragility, blistering, and photosensitivity. It is caused by mutations in the FBLIM1 gene, which encodes a protein called filamin B interacting protein 1.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for the identification of mutations or variations in the DNA sequence. In the context of Kindler syndrome, NGS genetic testing can be used to detect mutations in the FBLIM1 gene to confirm a diagnosis. This type of testing is particularly useful for rare genetic disorders like Kindler syndrome, as it allows for a comprehensive analysis of multiple genes at once.

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