Symptoms of COL11A1 Gene Marshall Syndrome Genetic Test
Marshall Syndrome, a genetic disorder caused by mutations in the COL11A1 gene, presents a variety of symptoms that can significantly impact an individual’s quality of life. Recognizing these symptoms early can lead to timely intervention and management. DNA Labs UAE offers a comprehensive genetic test for Marshall Syndrome, aiding in the diagnosis and understanding of this complex condition. The test is priced at 4400 AED, reflecting our commitment to providing accessible, high-quality genetic testing services.
Understanding Marshall Syndrome
Marshall Syndrome is a connective tissue disorder that shares similarities with Stickler Syndrome but is distinguished by its unique genetic cause: mutations in the COL11A1 gene. This gene plays a crucial role in the production of type XI collagen, a protein essential for the proper development of bones, eyes, ears, and other tissues. The mutation disrupts normal collagen production, leading to the various symptoms associated with the syndrome.
Key Symptoms of Marshall Syndrome
Individuals with Marshall Syndrome may exhibit a wide range of symptoms, varying in severity from one person to another. Key symptoms include:
- Sensorineural hearing loss: A common symptom that can range from mild to profound, affecting one’s ability to hear higher frequencies.
- Myopia and cataracts: Severe nearsightedness and early development of cataracts are hallmark signs of the syndrome.
- Flat midface and wide-set eyes: Facial features are distinct, with a flat appearance to the middle of the face and eyes that are set wider apart than usual.
- Skeletal abnormalities: Individuals may have shorter stature, spinal abnormalities, and joint issues.
- Dental problems: Abnormalities in tooth development and alignment are common.
Early detection and diagnosis are crucial for managing these symptoms effectively and improving the quality of life for individuals with Marshall Syndrome.
Genetic Testing for Marshall Syndrome at DNA Labs UAE
DNA Labs UAE is at the forefront of genetic diagnostics, offering a specialized COL11A1 Gene Marshall Syndrome Genetic Test designed to identify mutations in the COL11A1 gene. Priced at 4400 AED, this test is a vital tool for individuals experiencing symptoms of Marshall Syndrome or those with a family history of the condition. The test not only aids in the diagnosis but also helps in planning management strategies and understanding the risk of passing the mutation to future generations.
Why Choose DNA Labs UAE?
Choosing DNA Labs UAE for your genetic testing needs ensures access to state-of-the-art technology, highly qualified genetic counselors, and comprehensive support throughout the testing process. Our COL11A1 Gene Marshall Syndrome Genetic Test is conducted with the utmost care and precision, ensuring reliable results that can guide your healthcare decisions. With a clear focus on accessibility, we strive to make advanced genetic testing available to everyone in need.
For more information about the COL11A1 Gene Marshall Syndrome Genetic Test or to schedule a consultation, please visit our website.
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