Beta Thalassemia is a blood disorder that diminishes the production of hemoglobin, an iron-containing protein in red blood cells that carries oxygen to cells throughout the body. It is a genetic condition that involves the mutation of the HBB gene on chromosome 11, often leading to severe anemia, a condition where the body doesn’t have […]
Understanding the implications of genetic mutations is crucial in the realm of medical science, especially when it comes to diagnosing and treating various types of cancers. One such mutation that has garnered attention is the cKIT mutation, particularly in the context of Acute Myeloid Leukemia (AML). DNA Labs UAE is at the forefront of providing […]
Cystic fibrosis (CF) is a severe genetic disorder that affects the lungs, digestive system, and other organs. It results from mutations in the CFTR (cystic fibrosis transmembrane conductance regulator) gene, which leads to the production of thick, sticky mucus that can clog the airways and trap bacteria, leading to infections, inflammation, and other complications. Among […]
Symptoms of Prenatal Delta Beta-Thalassaemia Mutation Screening Test Delta Beta-Thalassaemia is a rare blood disorder that results from mutations affecting the production of hemoglobin, the protein in red blood cells responsible for carrying oxygen throughout the body. This condition can lead to anemia and other health issues, making early detection crucial for effective management. DNA […]
Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) are two forms of muscular dystrophy that are caused by mutations in the dystrophin gene. These conditions lead to muscle weakness and degeneration over time. The DMD/BMD Mutation Screening 26 Exons Test is a specialized genetic test designed to identify mutations in the 26 exons of […]
Ewing’s Sarcoma is a rare type of cancer that primarily affects bones but can also occur in the soft tissues surrounding the bones. This aggressive cancer is more common in children and teenagers and is characterized by the presence of a specific genetic anomaly involving the EWSR1 gene. DNA Labs UAE offers a comprehensive test […]
In the realm of medical genetics, understanding the nuances of specific mutations and their implications on health is paramount. Among these, the FLT3ITD mutation stands out due to its significant role in the development and prognosis of acute myeloid leukemia (AML). The FLT3ITD Allelic Ratio Test, offered by DNA Labs UAE, is a crucial diagnostic […]
Fragile X Syndrome (FXS) is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. It is the most common form of inherited intellectual disability in males and a significant cause of intellectual disability in females. The condition is caused by a mutation in the FMR1 gene on the […]
Huntington’s disease (HD) is a hereditary condition that causes the progressive breakdown of nerve cells in the brain. It has a significant impact on a person’s functional abilities, often resulting in movement, cognitive, and psychiatric disorders. With advancements in genetic testing, it is now possible to screen for the HD mutation, providing crucial information for […]
Symptoms of Mesoridazine Test Mesoridazine, a metabolite of thioridazine, is primarily used in the treatment of schizophrenia. It is a potent antipsychotic medication that works by altering the effects of chemicals in the brain. While effective, its use requires careful monitoring due to potential side effects and specific health risks associated with its administration. Recognizing […]
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.
