Fragile X Syndrome (FXS) is a genetic disorder that causes intellectual disability, behavioral and learning challenges, and various physical characteristics. It is the most common form of inherited intellectual disability in boys. The syndrome is related to the expansion of the CGG triplet repeat within the FMR1 gene on the X chromosome. Detecting this genetic […]
At DNA Labs UAE, we understand the importance of post-chemotherapy monitoring and the significant role it plays in a patient’s recovery journey. One of the critical tests we offer in this regard is the Large Biopsy 5 Post Chemotherapy Bone Test. This test is designed to assess the condition of the bones following chemotherapy treatment, […]
Symptoms of Alpha Thalassemia and the Importance of Mutation Screening Alpha Thalassemia is a blood disorder affecting the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. This condition results from mutations in the genes that control hemoglobin production, leading to anemia and other related health issues. Recognizing the […]
Beta Thalassemia is a genetic blood disorder that reduces the production of hemoglobin, the iron-containing protein in red blood cells that carries oxygen to cells throughout the body. Individuals with this condition experience an array of symptoms that can significantly impact their quality of life. Recognizing these symptoms early on is crucial for managing the […]
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 […]
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.
