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RAX2 Gene Cone-Rod Dystrophy Type 11 Genetic Test

4,400 د.إ

-21%

The RAX2 Gene Cone-Rod Dystrophy Type 11 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the RAX2 gene, which are implicated in the development of Cone-Rod Dystrophy Type 11. This condition is a rare form of inherited eye disorder that predominantly affects the cone and rod cells in the retina, leading to progressive vision loss. The test plays a crucial role in the early detection and management of the disorder, offering insights into potential treatments and interventions to slow the progression of the disease. The cost of the test is set at 4400 AED, reflecting the advanced genetic analysis involved in identifying the specific mutations within the RAX2 gene. Conducted in the state-of-the-art facilities of DNA Labs UAE, this genetic test is a significant step forward in personalized medicine, providing patients and their families with crucial information about their genetic health and the risk of inheriting or passing on Cone-Rod Dystrophy Type 11.

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RAX2 Gene Cone-rod dystrophy type 11 Genetic Test

Are you or a loved one experiencing progressive vision loss? It could be a symptom of cone-rod dystrophy type 11, a rare genetic disorder that affects the retina. The RAX2 Gene Cone-rod dystrophy type 11 Genetic Test offered by DNA Labs UAE can help provide early diagnosis and personalized treatment options.

Test Details

The RAX2 gene is associated with cone-rod dystrophy type 11, which specifically affects the retina – the light-sensitive tissue at the back of the eye. This disorder leads to progressive vision loss, starting with the cones (responsible for color vision and visual acuity) and later affecting the rods (responsible for low-light vision and peripheral vision).

Our NGS (Next-Generation Sequencing) technology allows us to analyze the DNA sequence of the RAX2 gene, identifying any changes or abnormalities that may be causing the symptoms of cone-rod dystrophy. This highly sensitive and accurate method for genetic analysis can detect even small changes in the DNA sequence, making it a valuable tool for diagnosing rare genetic disorders like cone-rod dystrophy type 11.

Components and Price

The RAX2 Gene Cone-rod dystrophy type 11 Genetic Test is priced at 4400.0 AED. The test can be conducted using a blood sample, extracted DNA, or just one drop of blood on an FTA Card.

Report Delivery and Method

After the test, the report will be delivered within 3 to 4 weeks. Our test utilizes NGS technology, ensuring accurate and reliable results.

Test Type and Doctor

The RAX2 Gene Cone-rod dystrophy type 11 Genetic Test falls under the category of Ophthalmology Disorders. It is recommended to consult with an Ophthalmologist, who will guide you through the testing process.

Test Department and Pre Test Information

The RAX2 Gene Cone-rod dystrophy type 11 Genetic Test is conducted in our Genetics department. Before the test, it is important to provide the clinical history of the patient and undergo a Genetic Counselling session to draw a pedigree chart of family members affected by RAX2 Gene Cone-rod dystrophy type 11.

Early diagnosis is crucial in managing cone-rod dystrophy type 11. The RAX2 Gene Cone-rod dystrophy type 11 Genetic Test offered by DNA Labs UAE can provide you with the answers you need for personalized treatment options. Contact us today to schedule your test.

Test Name RAX2 Gene Cone-rod dystrophy type 11 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 RAX2 Gene Cone-rod dystrophy type 11 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RAX2 Gene Cone-rod dystrophy type 11 NGS Genetic DNA Test gene RAX2
Test Details

The RAX2 gene is associated with cone-rod dystrophy type 11, a rare genetic disorder that affects the retina, the light-sensitive tissue at the back of the eye. This disorder is characterized by progressive vision loss, starting with the cones (the cells responsible for color vision and visual acuity) and later affecting the rods (the cells responsible for low-light vision and peripheral vision).

NGS (Next-Generation Sequencing) genetic testing can detect mutations in the RAX2 gene, allowing for early diagnosis and personalized treatment options. This test analyzes the DNA sequence of the RAX2 gene to identify any changes or abnormalities that may be causing the symptoms of cone-rod dystrophy.

NGS testing is a highly sensitive and accurate method for genetic analysis, allowing for the detection of even small changes in the DNA sequence. It is a useful tool for diagnosing rare genetic disorders, such as cone-rod dystrophy type 11, and can help guide treatment decisions and genetic counseling.