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 […]
In the realm of medical genetics, the discovery and understanding of specific gene mutations have paved the way for advanced diagnostic techniques and targeted treatment strategies. One such genetic condition that has garnered attention is the FLI1 gene platelet dense granule secretion defect, which can lead to excessive bleeding. DNA Labs UAE, a leading genetic […]
Understanding Thalassemia Alpha and the Role of the HBA1 Gene Thalassemia is a genetic blood disorder characterized by less oxygen-carrying hemoglobin and fewer red blood cells in the body than normal. Hemoglobin allows red blood cells to carry oxygen from your lungs to all parts of your body, and a deficiency can lead to anemia. […]
Symptoms of RUNX1 Gene Platelet Disorder with Associated Myeloid Malignancy Genetic Test The RUNX1 gene plays a pivotal role in the development of blood cells, and mutations in this gene can lead to a spectrum of hematological conditions. Among these, the RUNX1 gene platelet disorder with associated myeloid malignancy is of particular concern. This genetic […]
Thalassemia is a genetic blood disorder characterized by less oxygen-carrying hemoglobin and fewer red blood cells in the body than normal. Hemoglobin allows red blood cells to carry oxygen from your lungs to all parts of your body, and signs of thalassemia are linked to the lack of oxygen. Among the types of thalassemia, Alpha […]
The CD36 gene, also known as Platelet Glycoprotein IV, plays a crucial role in various bodily functions, including inflammation, lipid metabolism, and the immune response. Deficiency in the CD36 gene can lead to several health issues, primarily affecting the cardiovascular system, metabolic processes, and the body’s ability to fight infections. Recognizing the symptoms of CD36 […]
Symptoms of ITK Gene Lymphoproliferative Syndrome Type 1 Lymphoproliferative Syndrome Type 1, associated with mutations in the ITK gene, is a rare genetic disorder that affects the immune system. Individuals with this condition often experience a range of symptoms due to the abnormal proliferation of certain types of white blood cells. Recognizing these symptoms early […]
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.
