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SIX5 Gene Branchiootorenal Syndrome Type 2 Genetic Test

4,400 د.إ

-21%

The SIX5 Gene Branchiootorenal Syndrome Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the SIX5 gene, which are associated with Branchiootorenal Syndrome Type 2 (BOR2). BOR2 is a genetic condition characterized by developmental abnormalities affecting the ears, neck, and kidneys. Symptoms can vary widely among individuals but may include hearing loss, branchial cysts, renal anomalies, and other related issues.

This test is crucial for individuals with a family history of BOR2 or those exhibiting symptoms, as early diagnosis can lead to better management and treatment of the condition. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for genetic mutations in the SIX5 gene.

At DNA Labs UAE, the cost for the SIX5 Gene Branchiootorenal Syndrome Type 2 Genetic Test is set at 4400 AED. The price reflects the sophisticated technology and expertise required to accurately identify mutations in the gene of interest. By opting for this test, patients gain crucial insights into their genetic makeup, empowering them with the knowledge to make informed decisions about their health and the management of BOR2.

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  • This test is not intended for medical diagnosis or treatment
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SIX5 Gene Branchiootorenal syndrome type 2 Genetic Test

Welcome to DNA Labs UAE, your trusted genetic lab for all your testing needs. Today, we will be discussing the SIX5 Gene Branchiootorenal syndrome type 2 Genetic Test, its cost, symptoms, diagnosis, and other important details.

Test Name: SIX5 Gene Branchiootorenal syndrome type 2 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test type: Ophthalmology Disorders

Doctor: Ophthalmologist

Test Department: Genetics

Pre Test Information

Before undergoing the SIX5 Gene Branchiootorenal syndrome type 2 NGS Genetic DNA 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 the SIX5 Gene Branchiootorenal syndrome type 2 NGS Genetic DNA Test gene SIX5.

Test Details

The SIX5 gene is associated with Branchiootorenal syndrome type 2 (BOR2), an autosomal dominant disorder characterized by hearing loss and abnormalities of the kidneys, urinary tract, and neck. The SIX5 gene plays a crucial role in the development and function of the kidneys and inner ear. Mutations in the SIX5 gene can disrupt the normal function of the protein produced by this gene, resulting in the symptoms of BOR2.

NGS (next-generation sequencing) genetic testing is a highly advanced DNA sequencing method that allows for the rapid analysis of large amounts of genetic data. This type of testing can identify mutations in the SIX5 gene that are associated with BOR2. By undergoing NGS testing, individuals can receive a diagnosis for BOR2 and determine their risk of developing the condition. Furthermore, NGS testing can also be used to screen family members of affected individuals for the presence of the mutation.

At DNA Labs UAE, we prioritize accurate and timely genetic testing. Our SIX5 Gene Branchiootorenal syndrome type 2 Genetic Test is conducted using NGS technology, ensuring reliable results. Our team of genetics experts and ophthalmologists are dedicated to providing you with the highest level of care and support throughout the testing process.

If you have any questions or would like to schedule an appointment for the SIX5 Gene Branchiootorenal syndrome type 2 Genetic Test, please don’t hesitate to contact us. Your health and well-being are our top priorities.

Test Name SIX5 Gene Branchiootorenal syndrome type 2 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 Ophthalmology Disorders
Doctor Ophthalmologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SIX5 Gene Branchiootorenal syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SIX5 Gene Branchiootorenal syndrome type 2 NGS Genetic DNA Test gene SIX5
Test Details

The SIX5 gene is associated with Branchiootorenal syndrome type 2 (BOR2), which is an autosomal dominant disorder characterized by hearing loss and abnormalities of the kidneys, urinary tract, and neck. The SIX5 gene provides instructions for making a protein that is important for the development and function of the kidneys and inner ear. Mutations in the SIX5 gene can disrupt the normal function of this protein, leading to the signs and symptoms of BOR2.

NGS (next-generation sequencing) genetic testing is a type of DNA sequencing that can rapidly analyze large amounts of genetic data. NGS testing can be used to identify mutations in the SIX5 gene that are associated with BOR2. This type of testing can help diagnose BOR2 and identify individuals who are at risk of developing the condition. NGS testing can also be used to screen family members of affected individuals for the presence of the mutation.