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Connexin 30 Mutation Detection Test Cost

Original price was: 1,400 د.إ.Current price is: 1,260 د.إ.

-10%

The Connexin 30 Mutation Detection Test is a specialized genetic test available at DNA Labs UAE, designed to identify mutations in the GJB6 gene, which encodes the connexin 30 protein. This protein plays a crucial role in the formation of gap junctions that facilitate direct cellular communication in various tissues, including the inner ear and skin. Mutations in the GJB6 gene can lead to a range of disorders, most notably hearing impairments and certain skin conditions.

The test is particularly relevant for individuals with a family history of hearing loss or those experiencing symptoms without a clear diagnosis. Early detection through this test can aid in the understanding of the condition’s cause, enabling targeted interventions and informed decision-making regarding treatment options. It can also provide essential information for families considering future pregnancies.

Performed at DNA Labs UAE, a facility known for its advanced genetic testing services, the Connexin 30 Mutation Detection Test is priced at 1260 AED. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the GJB6 gene. Results from this test can offer valuable insights into the genetic basis of hearing loss and other related conditions, facilitating a personalized approach to healthcare.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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CONNEXIN 30 MUTATION DETECTION Test

At DNA Labs UAE, we offer the CONNEXIN 30 MUTATION DETECTION test, which is a genetic test used to detect mutations in the GJB6 gene. This gene is responsible for encoding the connexin 30 protein, and mutations in this gene have been associated with various conditions, including hearing loss and skin disorders.

Test Cost: AED 1260.0

Symptoms and Diagnosis

If you are experiencing symptoms related to connexin 30-related disorders, such as hearing loss or skin disorders, it is important to get tested. The CONNEXIN 30 MUTATION DETECTION test can help diagnose the underlying cause of your symptoms and determine your risk of developing certain conditions.

Test Components

  • Price: AED 1260.0
  • Sample Condition: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
  • Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.

Report Delivery

  • Sample Sat by 11 am
  • Report Working days

Method

The CONNEXIN 30 MUTATION DETECTION test is performed using PCR sequencing.

Test Type

The CONNEXIN 30 MUTATION DETECTION test is specifically designed to detect mutations related to neurologic disorders.

Doctor

This test can be ordered by a physician, neurologist, or ENT specialist.

Test Department

The CONNEXIN 30 MUTATION DETECTION test is conducted in our Molecular Diagnostics department.

Pre Test Information

A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for this test.

Test Details

The CONNEXIN 30 MUTATION DETECTION test involves analyzing a person’s DNA sample, typically obtained through a blood or saliva sample. The DNA is examined for specific mutations or changes in the GJB6 gene. If a mutation is detected, it can help diagnose the underlying cause of a person’s symptoms or determine their risk of developing certain conditions.

This test is typically ordered by a healthcare provider if there is a suspicion of a connexin 30-related disorder based on a person’s symptoms, family history, or other clinical findings. It can help guide treatment decisions and provide important information for genetic counseling.

It is important to note that this test specifically looks for mutations in the GJB6 gene and does not provide information about mutations in other genes that may also be involved in connexin-related disorders. Therefore, additional testing may be required if other genes are suspected to be involved.

Overall, the CONNEXIN 30 MUTATION DETECTION test plays a crucial role in diagnosing and managing connexin 30-related disorders, allowing for more personalized and targeted healthcare interventions.

Test Name CONNEXIN 30 MUTATION DETECTION Test
Components
Price 1260.0 AED
Sample Condition 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Report Delivery SampleSat by 11 am;Report Working days
Method PCR Sequencing
Test type Neurologic Disorder
Doctor Physician, Neurologist, ENT
Test Department: MOLECULAR DIAGNOSTICS
Pre Test Information Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Test Details

The CONNEXIN 30 MUTATION DETECTION test is a genetic test used to detect mutations in the GJB6 gene, which is responsible for encoding the connexin 30 protein. Mutations in this gene have been associated with various conditions, including hearing loss and skin disorders.

The test involves analyzing a person’s DNA sample, typically obtained through a blood or saliva sample. The DNA is examined for specific mutations or changes in the GJB6 gene. If a mutation is detected, it can help diagnose the underlying cause of a person’s symptoms or determine their risk of developing certain conditions.

The CONNEXIN 30 MUTATION DETECTION test is typically ordered by a healthcare provider if there is a suspicion of a connexin 30-related disorder based on a person’s symptoms, family history, or other clinical findings. It can help guide treatment decisions and provide important information for genetic counseling.

It is important to note that this test specifically looks for mutations in the GJB6 gene and does not provide information about mutations in other genes that may also be involved in connexin-related disorders. Therefore, additional testing may be required if other genes are suspected to be involved.

Overall, the CONNEXIN 30 MUTATION DETECTION test plays a crucial role in diagnosing and managing connexin 30-related disorders, allowing for more personalized and targeted healthcare interventions.