DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide patients and healthcare providers with critical information about genetic conditions. Among these, the CUL7 Gene Three M Syndrome Type 1 Genetic Test is a pivotal tool in diagnosing a rare genetic disorder that affects growth and development. This article delves into the symptoms of Three M Syndrome Type 1, the importance of genetic testing, and details regarding the test available at DNA Labs UAE, including its cost.
Symptoms of Three M Syndrome Type 1
Three M Syndrome is a rare genetic condition characterized by growth abnormalities, including short stature and skeletal anomalies. It is caused by mutations in the CUL7 gene, among others. Individuals with Three M Syndrome Type 1 typically present a range of symptoms that may vary in severity but often include:
- Significantly reduced growth both in utero and post-birth, leading to short stature.
- Distinguishing facial features such as a prominent forehead, full cheeks, and a triangular-shaped face.
- Skeletal abnormalities including a short neck, squared shoulders, and hyperlordosis (an exaggerated inward curve of the lower back).
- Delayed bone age.
- Intellectual development is typically normal, but some individuals may experience learning disabilities.
Importance of Genetic Testing for Three M Syndrome Type 1
Diagnosing Three M Syndrome Type 1 can be challenging due to its rarity and the variability of symptoms. Genetic testing, however, offers a definitive diagnosis by identifying mutations in the CUL7 gene. This is crucial for:
- Understanding the specific genetic alterations causing the condition.
- Guiding treatment and management plans tailored to the individual’s needs.
- Providing information on the risk of passing the condition to future offspring.
- Enabling families to connect with others affected by the syndrome and access supportive communities and resources.
The CUL7 Gene Three M Syndrome Type 1 Genetic Test at DNA Labs UAE
DNA Labs UAE provides a specialized genetic test to diagnose Three M Syndrome Type 1 by analyzing the CUL7 gene for mutations. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in our state-of-the-art laboratory. Our team of genetic experts ensures accurate and reliable results, enabling patients and their families to make informed decisions about their health and management of the condition.
Test Cost and Details
The cost of the CUL7 Gene Three M Syndrome Type 1 Genetic Test at DNA Labs UAE is 4400 AED. This includes the collection of the sample, the genetic analysis, and a comprehensive report detailing the findings. Our team is committed to providing support throughout the process, from initial consultation to post-test counseling.
For more information or to schedule a test, please visit our website at DNA Labs UAE – CUL7 Gene Three M Syndrome Type 1 Genetic Test.
In conclusion, the CUL7 Gene Three M Syndrome Type 1 Genetic Test is a vital tool in the diagnosis and management of Three M Syndrome. At DNA Labs UAE, we are dedicated to providing accurate genetic testing and support to individuals and families navigating this rare condition. By identifying the genetic basis of Three M Syndrome, we can empower patients with the knowledge to manage their health proactively.
