Shwachman-Diamond Syndrome (SDS) is a rare genetic disorder that affects multiple organs, including the bone marrow, pancreas, and skeletal system. It is primarily characterized by exocrine pancreatic insufficiency, bone marrow dysfunction, skeletal abnormalities, and an increased risk of developing myelodysplastic syndrome and acute myeloid leukemia. The syndrome is caused by mutations in the SBDS gene, […]
In the realm of medical genetics, the HBB gene sickle cell anemia genetic test emerges as a pivotal diagnostic tool, offering profound insights into one of the most common and severe genetic disorders worldwide. Sickle cell anemia, a condition marked by the production of abnormally shaped red blood cells, can lead to a myriad of […]
At DNA Labs UAE, we are committed to providing advanced genetic testing services to help diagnose and manage a variety of genetic conditions. One such condition is related to mutations in the TRNT1 gene, which can lead to a complex syndrome characterized by sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay. Understanding the symptoms […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals understand their genetic makeup and manage their health better. One of the specialized tests we offer is the ANK1 Gene Spherocytosis Type 1 Genetic Test. This test is crucial for diagnosing Hereditary Spherocytosis (HS), a condition that affects the […]
Spherocytosis Type 2, caused by mutations in the SPTB gene, is a genetic condition characterized by the presence of spherocytes (sphere-shaped red blood cells) in the blood, leading to various symptoms and complications. Recognizing the importance of early diagnosis and intervention, DNA Labs UAE offers a comprehensive genetic test for this condition. Understanding the symptoms […]
Spherocytosis is a form of anemia characterized by the presence of spherocytes, or spherical red blood cells, in the bloodstream. This condition is caused by a variety of genetic mutations that affect the proteins responsible for maintaining the red blood cells’ shape and flexibility. Among these genetic mutations, the SPTA1 gene plays a crucial role, […]
Understanding CSF3R Gene Neutrophilia Hereditary Genetic Test Neutrophilia, a condition characterized by an abnormally high number of neutrophils in the bloodstream, can be a response to various factors, including infections, inflammation, and certain drugs. However, when neutrophilia is hereditary, it is often linked to mutations in the CSF3R gene. The CSF3R gene plays a critical […]
At DNA Labs UAE, we are committed to providing our clients with comprehensive and reliable genetic testing services. One of the specialized tests we offer is for the diagnosis of Spherocytosis Type 5, which is caused by mutations in the EPB42 gene. This condition is a rare form of hereditary spherocytosis, a disorder that affects […]
Platelet aggregation disorders are a group of bleeding disorders that affect the way your platelets clump together, or aggregate. One such disorder is associated with mutations in the PEAR1 gene. Understanding the symptoms of this condition is crucial for early diagnosis and treatment. DNA Labs UAE offers a genetic test specifically designed to identify mutations […]
Stormorken Syndrome is a rare genetic disorder that affects multiple systems within the body, leading to a variety of symptoms. It is caused by mutations in the STIM1 gene, which plays a critical role in calcium signaling within cells. This signaling is crucial for the proper functioning of muscle cells, blood cells, and other types […]
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.
