DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of tests designed to provide individuals with crucial information about their genetic makeup. Among these tests, the CCDC40 Gene Primary Ciliary Dyskinesia Type 15 Genetic Test stands out due to its importance in diagnosing a specific form of Primary Ciliary Dyskinesia […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, the microscopic, hair-like structures that line the airways, ears, and other parts of the body. These cilia play a crucial role in moving mucus towards the throat, where it can be either coughed up or swallowed. When cilia do not function properly, […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, the tiny hair-like structures that line the airways, ears, and other parts of the body. These cilia play a crucial role in moving mucus and other substances out of the lungs, respiratory tract, and other areas. When cilia do not function properly […]
Primary Ciliary Dyskinesia (PCD) is a rare, inherited, genetic disorder that affects the function of cilia in the human body. Cilia are tiny, hair-like structures that line various organs, including the lungs, nose, and ears. They play a crucial role in moving mucus and other substances through the airways, protecting the lungs from infection and […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, tiny hair-like structures that line the airways, ears, and other parts of the body. These cilia play a crucial role in moving mucus and other materials out of the airways, ears, and sinuses. When cilia do not work properly due to genetic […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the function of cilia, the microscopic, hair-like structures that line the airways, reproductive system, and other parts of the body. The DNAI2 gene plays a crucial role in the development and function of these cilia. Mutations in the DNAI2 gene can lead to Primary […]
In the realm of genetic diagnostics and personalized medicine, understanding and identifying genetic disorders early on can significantly improve the management and prognosis of affected individuals. One such condition, Primary Ciliary Dyskinesia (PCD) Type 18, caused by mutations in the DNAAF5 gene, is a rare but significant disorder that impacts the respiratory system, fertility, and […]
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the cilia, the microscopic, hair-like structures that line the airways, ears, and other parts of the body. These cilia play a crucial role in moving mucus and other materials out of the respiratory tract, ensuring the proper functioning of the respiratory system. One specific […]
In the realm of genetic diagnostics, the pursuit of understanding and identifying the root causes of complex conditions has led to the development of sophisticated genetic tests. One such pivotal test is the TIMM8A Gene Opticoacoustic Nerve Atrophy with Dementia Genetic Test, offered by DNA Labs UAE. This specific examination is designed to detect mutations […]
Otopalatodigital syndrome type 1 (OPD1) is a rare genetic disorder that affects bone growth and development, leading to skeletal abnormalities and a range of other potential physical issues. This condition is caused by mutations in the FLNA gene, which plays a critical role in cell structure and movement. Understanding the symptoms of this disorder is […]
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.
