Symptoms of FGFR2 Gene Apert Syndrome Genetic Test Apert Syndrome is a genetic disorder that results from the mutation of the FGFR2 (Fibroblast Growth Factor Receptor 2) gene. This rare condition is characterized by the premature fusion of certain skull bones (craniosynostosis), which affects the shape of the head and face. Additionally, individuals with Apert […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help identify various genetic disorders, including those detected through the Dysmorphology Panel NGS Genetic Test. This advanced genetic test plays a crucial role in diagnosing congenital anomalies and developmental disorders, offering hope and direction for affected individuals and their families. Understanding […]
— Ciliopathies are a group of rare genetic disorders caused by defects in the structure or function of cilia, which are microscopic, hair-like structures on the surface of cells. These disorders can affect multiple systems in the body, leading to a wide range of symptoms. The Ciliopathies Panel NGS (Next-Generation Sequencing) Genetic Test is a […]
Understanding the symptoms associated with Noonan Syndrome and related RASopathies is crucial for early diagnosis and intervention. Noonan Syndrome, along with a spectrum of other conditions known as RASopathies, are genetic disorders that can have a significant impact on an individual’s health and development. These conditions are caused by mutations in genes that are part […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
