Symptoms and Testing information for FKBP10 Gene Osteogenesis Imperfecta Type 11 Genetic Test

Symptoms and Testing information for FKBP10 Gene Osteogenesis Imperfecta Type 11 Genetic Test

Osteogenesis Imperfecta (OI) is a group of genetic disorders that mainly affect the bones, making them fragile and more likely to break. Among the various types of OI, Type 11 is particularly notable for its association with mutations in the FKBP10 gene. This article delves into the symptoms of FKBP10 gene Osteogenesis Imperfecta Type 11 and the genetic testing available for this condition, specifically highlighting the test offered by DNA Labs UAE for a cost of 4400 AED.

Symptoms of FKBP10 Gene Osteogenesis Imperfecta Type 11

Osteogenesis Imperfecta Type 11 is a rare form of the condition that presents several unique symptoms alongside the common characteristics of OI. Individuals with this type may experience:

  • Increased bone fragility leading to frequent fractures with minimal or no trauma.
  • Blue sclera, which is the white part of the eye turning blue or grey.
  • Hearing loss, which can be progressive and affect individuals from a young age.
  • Skeletal deformities, including bowing of the legs, scoliosis, and chest deformities.
  • Joint hypermobility, leading to joints that are more flexible than usual.
  • Dentinogenesis imperfecta, affecting the development of teeth and making them discolored, brittle, and prone to wear and breakage.

These symptoms can vary significantly in severity among individuals, with some experiencing mild symptoms and others facing severe physical limitations.

Genetic Testing for FKBP10 Gene Osteogenesis Imperfecta Type 11

Genetic testing plays a crucial role in diagnosing Osteogenesis Imperfecta Type 11, enabling accurate diagnosis and appropriate management of the condition. DNA Labs UAE offers a comprehensive genetic test specifically designed to detect mutations in the FKBP10 gene associated with OI Type 11. The cost of this test is 4400 AED.

This genetic test involves analyzing the patient’s DNA to identify mutations in the FKBP10 gene. A positive result indicates the presence of a mutation that is known to cause OI Type 11, confirming the diagnosis. This information is invaluable for affected individuals and their families as it provides a clear understanding of the condition, guiding treatment decisions and management strategies.

Why Choose DNA Labs UAE for Your Genetic Testing?

DNA Labs UAE is a leading provider of genetic testing services, offering accurate and reliable results. The laboratory is equipped with state-of-the-art technology and staffed by experienced professionals who are committed to providing high-quality care. Choosing DNA Labs UAE for FKBP10 gene Osteogenesis Imperfecta Type 11 genetic testing ensures:

  • Accurate and reliable detection of mutations in the FKBP10 gene.
  • Comprehensive support from a team of experts who specialize in genetic disorders.
  • Confidential handling of all genetic information and test results.
  • Competitive pricing, with the test available for 4400 AED.

For more information about the FKBP10 gene Osteogenesis Imperfecta Type 11 genetic test and to schedule your testing, please visit DNA Labs UAE.

Understanding the genetic basis of Osteogenesis Imperfecta Type 11 through genetic testing can significantly impact the lives of those affected by the condition. It not only confirms the diagnosis but also facilitates targeted management and treatment strategies, improving the quality of life for individuals and their families. With advancements in genetic testing, such as the services offered by DNA Labs UAE, there is hope for better outcomes for those living with this challenging condition.

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