Symptoms and Testing information for FGFRL1 Gene Radioulnar Synostosis FGFRL1 Related Genetic Test

Symptoms and Testing information for FGFRL1 Gene Radioulnar Synostosis FGFRL1 Related Genetic Test

Radioulnar synostosis is a rare genetic condition characterized by the fusion of the radius and ulna bones in the forearm, leading to limitations in forearm movement and a range of motion. This condition can significantly impact an individual’s quality of life, making early diagnosis and understanding of the genetic basis crucial for management and treatment options. The FGFRL1 gene has been associated with this condition, and advancements in genetic testing have made it possible to identify mutations in this gene that may lead to radioulnar synostosis. DNA Labs UAE offers a comprehensive genetic test specifically designed to identify mutations in the FGFRL1 gene related to this condition.

Symptoms of FGFRL1 Gene Radioulnar Synostosis

Individuals with mutations in the FGFRL1 gene and radioulnar synostosis typically exhibit a range of symptoms that can vary in severity. Common symptoms include:

  • Limited ability to rotate the forearm, which may affect both supination (turning the palm upward) and pronation (turning the palm downward).
  • Visible deformity in the forearm due to the fusion of the radius and ulna bones.
  • Possible discrepancy in arm length, with the affected arm often being shorter.
  • Difficulty in performing tasks that require twisting motions of the arm, such as opening doors or using screwdrivers.

It’s important to note that the severity of symptoms can vary widely among individuals, with some experiencing minimal impact on daily activities, while others may face significant challenges.

FGFRL1 Related Genetic Test

DNA Labs UAE offers a specialized genetic test aimed at identifying mutations in the FGFRL1 gene that are linked to radioulnar synostosis. This test is an invaluable tool for individuals with a family history of the condition or who exhibit symptoms associated with it. Early detection through genetic testing can facilitate better management strategies and inform decisions regarding potential interventions.

Test Cost

The cost of the FGFRL1 gene radioulnar synostosis-related genetic test at DNA Labs UAE is 4400 AED. While the test represents a significant investment, the insights it provides into managing the condition and making informed health decisions can be invaluable.

Why Choose DNA Labs UAE?

DNA Labs UAE is a leading provider of genetic testing services in the region, offering a wide range of tests designed to uncover genetic predispositions and conditions. The laboratory is equipped with state-of-the-art technology and staffed by a team of experts in the field of genetics. Choosing DNA Labs UAE for your genetic testing needs ensures accurate, reliable results and comprehensive support throughout the testing process.

For more information about the FGFRL1 gene radioulnar synostosis-related genetic test and to schedule your test, please visit https://dnalabsuae.com/tests/fgfrl1-gene-radioulnar-synostosis-fgfrl1-related-genetic-test/.

Understanding your genetic makeup and identifying potential health risks associated with conditions like radioulnar synostosis can empower you to make informed decisions about your health and wellbeing. With advancements in genetic testing, individuals now have access to crucial information that can guide their healthcare journey. DNA Labs UAE is committed to providing accurate, comprehensive genetic testing services to help you navigate your health with confidence.

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