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GDF3 Gene Klippel-Feil Syndrome Type 3 Autosomal Dominant Genetic Test Cost

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

-21%

The GDF3 gene is associated with Klippel-Feil Syndrome Type 3, a condition characterized by the congenital fusion of any two of the seven cervical vertebrae. It is a form of skeletal anomaly that leads to a limited range of motion in the neck and can be accompanied by other developmental issues in the body. The condition is inherited in an autosomal dominant pattern, meaning that only one copy of the altered gene in each cell is sufficient to cause the disorder.

To diagnose this specific subtype of Klippel-Feil Syndrome, genetic testing focusing on the GDF3 gene is essential. This test can confirm the presence of mutations in the GDF3 gene that are known to cause the syndrome. Conducting this test is crucial for accurate diagnosis, informed decision-making regarding treatment options, and understanding the risk of passing the condition on to future generations.

In the UAE, DNA Labs offers this specialized genetic test for Klippel-Feil Syndrome Type 3. The test cost is set at 4400 AED. DNA Labs UAE is equipped with advanced genetic testing technologies and staffed by professionals skilled in conducting and interpreting these tests. Opting for this test at DNA Labs UAE ensures a comprehensive analysis of the GDF3 gene to ascertain the genetic basis of the condition in affected individuals or families with a history of Klippel-Feil Syndrome.

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GDF3 Gene Klippel-Feil Syndrome Type 3 Autosomal Dominant Genetic Test

At DNA Labs UAE, we offer the GDF3 Gene Klippel-Feil syndrome type 3 autosomal dominant genetic test. This test helps in diagnosing individuals with Klippel-Feil syndrome type 3, which is an autosomal dominant disorder.

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

Before undergoing the GDF3 Gene Klippel-Feil syndrome type 3 autosomal dominant genetic test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with GDF3 Gene Klippel-Feil syndrome type 3 autosomal dominant NGS genetic DNA test gene GDF3.

Test Details

The GDF3 gene is associated with Klippel-Feil syndrome type 3, an autosomal dominant disorder. Our NGS (Next-Generation Sequencing) genetic testing method analyzes the DNA sequence of an individual’s genes to identify any genetic variations or mutations related to this condition. By analyzing the GDF3 gene, we can diagnose individuals with Klippel-Feil syndrome type 3 and provide valuable information for genetic counseling and management of the disorder.

It is important to note that genetic testing should always be done under the guidance of a healthcare professional or genetic counselor. They can interpret the results and provide appropriate counseling and support.

Test Name GDF3 Gene Klippel-Feil syndrome type 3 autosomal dominant 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 GDF3 Gene Klippel-Feil syndrome type 3, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GDF3 Gene Klippel-Feil syndrome type 3, autosomal dominant NGS Genetic DNA Test gene GDF3
Test Details

The GDF3 gene is associated with Klippel-Feil syndrome type 3, which is an autosomal dominant disorder. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes to identify any genetic variations or mutations that may be associated with a particular condition or disorder.

In the context of Klippel-Feil syndrome type 3, NGS genetic testing can be used to analyze the GDF3 gene for any mutations or variations that may be present. This can help in diagnosing individuals with the condition and also provide valuable information for genetic counseling and management of the disorder.

It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and support.