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GDF6 Gene Klippel-Feil Syndrome Type 1 Autosomal Dominant Genetic Test

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

-21%

The GDF6 Gene Klippel-Feil Syndrome Type 1 Autosomal Dominant Genetic Test is a specialized diagnostic examination offered at DNA Labs UAE, aimed at identifying mutations in the GDF6 gene which are associated with Klippel-Feil Syndrome Type 1. Klippel-Feil Syndrome is a rare congenital condition characterized by the fusion of two or more cervical vertebrae, leading to a variety of symptoms including a limited range of neck motion, short neck, and low hairline at the back of the head. As an autosomal dominant condition, having a mutation in just one of the two copies of the GDF6 gene is sufficient to cause the syndrome.

The test, priced at 4400 AED, involves collecting a DNA sample from the patient, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect the presence of genetic mutations in the GDF6 gene. This genetic testing is crucial for accurate diagnosis, guiding treatment decisions, and providing information on the risk of passing the condition to future generations. Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities and comprehensive diagnostic services, this test represents a critical step for individuals suspected of having Klippel-Feil Syndrome Type 1 or those with a family history of the condition, seeking to understand their genetic health.

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GDF6 Gene Klippel-Feil syndrome type 1 autosomal dominant Genetic Test

Welcome to DNA Labs UAE, where we offer the GDF6 Gene Klippel-Feil syndrome type 1 autosomal dominant Genetic Test. This test is designed to analyze the GDF6 gene and identify any potential mutations or variations associated with Klippel-Feil syndrome type 1.

Test Components and Price

Test Name: GDF6 Gene Klippel-Feil syndrome type 1 autosomal dominant 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 and Test Department

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information

Clinical History of Patient who is going for GDF6 Gene Klippel-Feil syndrome type 1, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GDF6 Gene Klippel-Feil syndrome type 1, autosomal dominant NGS Genetic DNA Test gene GDF6

Test Details

The GDF6 gene is associated with Klippel-Feil syndrome type 1, which is an autosomal dominant disorder. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the GDF6 gene and identify any potential mutations or variations that may be present. NGS genetic testing involves sequencing the entire GDF6 gene to detect any changes in the DNA sequence. This can help in diagnosing individuals with Klippel-Feil syndrome type 1 and also provide information about the specific genetic variant causing the condition. By identifying the specific genetic variant, NGS testing can provide valuable information for genetic counseling, family planning, and potentially targeted treatment options. It can also help in understanding the underlying molecular mechanisms of Klippel-Feil syndrome type 1 and contribute to further research in the field. It is important to consult with a healthcare professional or genetic counselor before undergoing any genetic testing to understand the implications, limitations, and potential benefits of the test.

Test Name GDF6 Gene Klippel-Feil syndrome type 1 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 GDF6 Gene Klippel-Feil syndrome type 1, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GDF6 Gene Klippel-Feil syndrome type 1, autosomal dominant NGS Genetic DNA Test gene GDF6
Test Details

The GDF6 gene is associated with Klippel-Feil syndrome type 1, which is an autosomal dominant disorder. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the GDF6 gene and identify any potential mutations or variations that may be present.

NGS genetic testing involves sequencing the entire GDF6 gene to detect any changes in the DNA sequence. This can help in diagnosing individuals with Klippel-Feil syndrome type 1 and also provide information about the specific genetic variant causing the condition.

By identifying the specific genetic variant, NGS testing can provide valuable information for genetic counseling, family planning, and potentially targeted treatment options. It can also help in understanding the underlying molecular mechanisms of Klippel-Feil syndrome type 1 and contribute to further research in the field.

It is important to consult with a healthcare professional or genetic counselor before undergoing any genetic testing to understand the implications, limitations, and potential benefits of the test.