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 […]
Understanding the intricacies of genetic conditions is crucial for effective diagnosis and management. Among these conditions, X-Linked Protoporphyria, caused by mutations in the ALAS2 gene, stands out due to its distinct symptoms and inheritance pattern. DNA Labs UAE is at the forefront of diagnosing this condition through the ALAS2 Gene Protoporphyria Erythropoietic X-Linked Genetic Test. […]
Understanding the complexities of genetic disorders is crucial for early diagnosis and treatment. Among these disorders, one that stands out due to its rarity and multifaceted nature is the GGCX gene pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency. This condition, though not widely known, can have significant implications on an individual’s health, making awareness […]
Schimke immunoosseous dysplasia (SIOD) is a rare, autosomal recessive disorder characterized by spondyloepiphyseal dysplasia, renal disease, and T-cell immunodeficiency. It is caused by mutations in the SMARCAL1 gene. Recognizing the symptoms of SIOD is critical for early diagnosis and management of the condition. DNA Labs UAE offers a comprehensive genetic test for the SMARCAL1 gene […]
— Severe Combined Immunodeficiency (SCID) is a rare genetic disorder that significantly affects the immune system, leaving individuals extremely vulnerable to infections. Among the various forms of SCID, the JAK3 gene SCID Autosomal Recessive T Negative B Positive Type is notable. This condition is characterized by the absence or malfunctioning of immune cells known as […]
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.
