Fanconi-Bickel Syndrome (FBS) is a rare genetic disorder that affects the body’s ability to properly metabolize and utilize carbohydrates, leading to a range of health issues, from poor growth to rickets. At the core of this condition is a mutation in the SLC2A2 gene, which plays a crucial role in glucose transport within the body. […]
Fanconi Renotubular Syndrome Type 2, also known as Fanconi Syndrome, is a rare genetic disorder that affects the kidneys’ ability to reabsorb essential substances into the bloodstream. This condition is primarily caused by mutations in the SLC34A1 gene, which plays a crucial role in phosphate absorption and regulation in the kidneys. Understanding the symptoms of […]
In the realm of genetic testing, advancements have paved the way for the identification and understanding of various genetic conditions that were once shrouded in mystery. Among these, the F13A1 gene factor XIIIA deficiency stands out due to its critical role in the blood coagulation process. At DNA Labs UAE, we are at the forefront […]
— Understanding the Symptoms of F12 Gene Factor XII Deficiency and the Importance of Genetic Testing Factor XII deficiency, also known as Hageman factor deficiency, is a rare genetic disorder that affects the blood’s ability to clot. This condition is caused by mutations in the F12 gene, which plays a crucial role in the coagulation […]
At DNA Labs UAE, we are committed to providing our clients with comprehensive genetic testing services to identify various conditions, including the F11 Gene Factor XI Deficiency. This particular test is crucial for individuals who might be at risk of this genetic disorder, which can significantly impact their health and quality of life. Understanding the […]
Symptoms of ESR1 Gene Estrogen Resistance Genetic Test The ESR1 gene plays a pivotal role in mediating the effects of estrogen, a crucial hormone in the development and function of both female and male reproductive systems. Mutations in the ESR1 gene can lead to estrogen resistance, a rare condition that can have significant implications on […]
Understanding the nuances of genetic disorders is pivotal in the realm of modern medicine, and the MYH9 Gene Epstein Syndrome is one such condition that demands attention. This syndrome is a result of mutations in the MYH9 gene, which plays a crucial role in the formation and function of platelets and white blood cells. Recognizing […]
Endocrine-Cerebroosteodysplasia (ECO) is a rare, complex genetic condition that affects various systems within the body, including the endocrine system, brain, and bones. This disorder is caused by mutations in the ICK gene, which plays a significant role in cellular processes such as cell division and development. Understanding the symptoms associated with this genetic condition is […]
Dubin-Johnson Syndrome (DJS) is a rare genetic disorder characterized by chronic jaundice. This condition arises due to a mutation in the ABCC2 gene, which plays a crucial role in the secretion of conjugated bilirubin from hepatocytes into the bile. The ABCC2 gene Dubin-Johnson Syndrome Genetic Test is a pivotal step towards diagnosing this condition, enabling […]
— Understanding the nuances of genetic conditions is crucial for effective diagnosis and management. Among these, Nephrogenic Diabetes Insipidus (NDI) represents a unique challenge. It is a rare disorder affecting the kidneys’ ability to concentrate urine, leading to excessive urination and thirst. This condition is often linked to mutations in the AQP2 gene, which encodes […]
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.
