Achondroplasia is a common form of dwarfism that affects approximately 1 in 25,000 newborns worldwide. It is characterized by a specific set of physical features and health complications, most of which are attributed to mutations in the FGFR3 gene. The G1138A and G1138C mutations within this gene are among the most prevalent causes of this […]
Alveolar rhabdomyosarcoma (ARMS) is a rare and aggressive form of soft tissue sarcoma that predominantly affects children and young adults. It is characterized by the presence of specific genetic abnormalities, one of which involves the FOXO1 gene. The FOXO1 Break Apart FISH (Fluorescence In Situ Hybridization) Alveolar Rhabdomyosarcoma Diagnostic Test is a critical tool in […]
Detecting the presence of specific genetic markers can be crucial in diagnosing and treating various health conditions. One such marker is the BCL2IGH t(14;18) translocation, which is often associated with certain types of lymphoma, particularly non-Hodgkin lymphoma. Understanding the symptoms and getting tested can be a vital step in early detection and management of the […]
Understanding the significance of BCL6 tests is crucial in the realm of medical diagnostics, particularly when it comes to identifying specific health conditions. The BCL6 gene plays a pivotal role in the immune system, impacting various biological processes. Abnormalities in the BCL6 gene can lead to a range of health issues, making the BCL6 test […]
Understanding the nuances of genetic disorders and mutations is crucial for early detection, effective treatment, and better management of various diseases. Among the significant genetic markers that have been studied for their implications in health is the BCR-ABL gene rearrangement. This genetic anomaly is primarily associated with chronic myeloid leukemia (CML) and, to a lesser […]
Symptoms of BCR-ABL1 Quantification by DD PCR Test The BCR-ABL1 gene fusion is a hallmark of chronic myeloid leukemia (CML) and, to a lesser extent, acute lymphoblastic leukemia (ALL). This genetic anomaly results from the translocation between chromosome 9 and chromosome 22, known as the Philadelphia chromosome. The detection and quantification of the BCR-ABL1 fusion […]
In the realm of genetic testing, the BCR-ABL1 Quantitative p210p190p230 Test stands out as a pivotal diagnostic tool, especially in the detection and monitoring of certain types of leukemia. This test is particularly essential for individuals suspected of having Chronic Myeloid Leukemia (CML) or Acute Lymphoblastic Leukemia (ALL), as it helps in identifying the presence […]
Beta Thalassemia is a blood disorder that diminishes the production of hemoglobin, the iron-containing protein in red blood cells that carries oxygen to cells throughout the body. Individuals with beta thalassemia diseases have a reduced ability to produce beta-globin, a component of hemoglobin. This condition can lead to anemia, a condition characterized by fatigue and […]
In the realm of medical diagnostics, the BK virus (BKV) poses a unique challenge due to its latent nature in most individuals. It becomes a matter of concern primarily in immunocompromised patients, where it can lead to significant morbidity. The BKJC Qualitative PCR Test is a pivotal tool in diagnosing infections caused by the BK […]
In the realm of genetic testing, understanding the intricacies of our chromosomes is crucial for early diagnosis and intervention in various genetic disorders. The chromosomes 13, 18, 21, X, and Y are particularly significant due to their association with several well-known chromosomal abnormalities. At DNA Labs UAE, we offer a comprehensive test that examines these […]
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.
