Hematology Diseases

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 […]

At DNA Labs UAE, we are committed to providing our clients with the most comprehensive genetic testing services, including the APOE Gene Sea-Blue Histiocyte Disease Genetic Test. This particular test is essential for individuals who are at risk of developing Sea-Blue Histiocyte Syndrome, a rare genetic disorder. By understanding the symptoms associated with this condition […]

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 […]

Hemophilia B, also known as Christmas disease, is a genetic disorder that leads to impaired blood clotting. This condition, caused by mutations in the Factor IX (F9) gene, results in a deficiency of Factor IX, a protein crucial for blood clotting. Recognizing the symptoms early can be vital for effective management and treatment. DNA Labs […]