Symptoms and Testing information for PROM1 Gene Cone-Rod Dystrophy Type 12 Genetic Test

Symptoms and Testing information for PROM1 Gene Cone-Rod Dystrophy Type 12 Genetic Test

Cone-rod dystrophy type 12 is a severe genetic disorder that affects the eyes, leading to a progressive loss of vision. This condition is caused by mutations in the PROM1 gene, which plays a crucial role in the normal functioning of the photoreceptors in the retina. The photoreceptors are responsible for capturing light and converting it into electrical signals that the brain interprets as visual images. When these cells malfunction due to genetic mutations, it results in vision impairment and, ultimately, blindness. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a genetic test specifically designed to identify mutations in the PROM1 gene, aiding in the diagnosis of cone-rod dystrophy type 12.

Symptoms of PROM1 Gene Cone-Rod Dystrophy Type 12

The symptoms of cone-rod dystrophy type 12 typically manifest in childhood or early adolescence, but the onset and severity can vary widely among individuals. The primary symptoms include:

  • Diminished visual acuity: Individuals may struggle to see details clearly, affecting both near and far vision.
  • Decreased sensitivity to light: Patients often experience difficulty adapting to changes in light conditions, particularly in bright environments.
  • Loss of color vision: The ability to distinguish colors diminishes as the cones in the retina deteriorate.
  • Progressive vision loss: Over time, individuals experience a broad decline in their field of vision, which can lead to tunnel vision or complete blindness.
  • Night blindness: The rods, responsible for vision in low light, also deteriorate, making it challenging to see in dim conditions.

It’s important to note that these symptoms can lead to significant challenges in daily activities, affecting an individual’s quality of life and independence.

Genetic Test for PROM1 Gene Cone-Rod Dystrophy Type 12

DNA Labs UAE offers a comprehensive genetic test designed to detect mutations in the PROM1 gene. This test is a critical tool for diagnosing cone-rod dystrophy type 12, allowing for early intervention and management strategies to be implemented. The test involves a simple blood draw or cheek swab, with samples then analyzed in our state-of-the-art laboratory.

Cost of the Test

The cost of the PROM1 gene cone-rod dystrophy type 12 genetic test at DNA Labs UAE is 4400 AED. This investment covers the full cost of the test, including the analysis and a detailed report of the findings. Our team of genetic counselors is also available to discuss the results and provide guidance on the next steps.

Why Choose DNA Labs UAE?

Choosing DNA Labs UAE for your genetic testing needs ensures that you receive accurate and reliable results. Our laboratory is equipped with the latest technology, and our team of experts is dedicated to providing high-quality services. We understand the importance of privacy and confidentiality and uphold the highest standards to protect our clients’ information.

Conclusion

Understanding the symptoms of cone-rod dystrophy type 12 and undergoing genetic testing if these symptoms are present can be crucial steps in managing this condition. The PROM1 gene cone-rod dystrophy type 12 genetic test offered by DNA Labs UAE is a valuable resource for individuals and families affected by this disorder. By identifying mutations in the PROM1 gene, patients can gain insights into their condition and explore potential treatment and management options.

For more information on the PROM1 gene cone-rod dystrophy type 12 genetic test and to schedule your test, please visit https://dnalabsuae.com/tests/prom1-gene-cone-rod-dystrophy-type-12-genetic-test/.

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