Chromosome Breakage Syndrome is a group of disorders characterized by the tendency of chromosomes to break more easily than normal. This increased susceptibility to breakage can lead to a variety of clinical manifestations, including developmental delays, intellectual disabilities, congenital anomalies, and an increased risk of cancer. Understanding the symptoms and undergoing timely testing can play […]
DNA Labs UAE is at the forefront of genetic testing, offering a wide range of services aimed at providing accurate and vital information that can significantly impact individuals’ health and treatment options. Among the various tests available, the C-Myc Oncogene Test is one of the critical analyses performed by DNA Labs UAE, designed to detect […]
Erythropoietin (EPO) is a hormone produced by the kidneys that regulates red blood cell production in the bone marrow. Mutations in the Erythropoietin Receptor (EPOR) gene can lead to various hematologic disorders, affecting the body’s ability to produce red blood cells efficiently. Understanding the symptoms of EPOR gene mutations is crucial for timely diagnosis and […]
In the realm of personalized medicine and targeted therapy, understanding the genetic underpinnings of cancer has become crucial. One such advancement is the identification and testing for FGFR1 (Fibroblast Growth Factor Receptor 1) abnormalities in solid tumors. DNA Labs UAE stands at the forefront of this innovation, offering comprehensive FGFR1 Solid Tumor Tests. This test […]
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 […]
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.
