Understanding Galactosemia Epimerase Deficiency Galactosemia Epimerase Deficiency is a rare genetic disorder that affects an individual’s ability to process galactose, a sugar found in milk and other dairy products. This condition is caused by a deficiency in the enzyme known as UDP-galactose-4-epimerase, which plays a critical role in the conversion of galactose to glucose in […]
Blogs
Symptoms and Testing information for DHEA Dehydroepiandrosterone Test
In the realm of hormonal health and wellness, understanding the intricacies of our body’s biochemistry is paramount. Among the myriad hormones that orchestrate the symphony of our physiological processes, Dehydroepiandrosterone (DHEA) plays a crucial role. Produced by the adrenal glands, DHEA serves as a precursor to male and female sex hormones, including testosterone and estrogen. […]
Symptoms and Testing information for Anti-ss DNA Antibody Test
Understanding Anti-ss DNA Antibody Test Autoimmune diseases present a complex challenge in the medical field, often requiring precise diagnostic tools for accurate management and treatment. One such pivotal diagnostic tool is the Anti-ss DNA Antibody Test, a specific examination designed to detect the presence of antibodies against single-stranded DNA (ssDNA) in the blood. These antibodies […]
Symptoms and Testing information for Antenatal Panel 1 Test
Symptoms of Antenatal Panel 1 Test Pregnancy is a time of great joy and anticipation for expectant parents. However, it also comes with the responsibility of ensuring the health and well-being of both the mother and the baby. This is where antenatal screening tests play a crucial role. Among these, the Antenatal Panel 1 Test […]
Symptoms and Testing information for TORCH Panel IgG and IgM Test
In the realm of prenatal and neonatal healthcare, the TORCH Panel IgG and IgM Test emerges as a pivotal diagnostic tool. This comprehensive screening test is designed to detect infections that could potentially harm an unborn child or newborn, including Toxoplasmosis, Other agents (like Syphilis, Varicella-Zoster, Parvovirus B19), Rubella, Cytomegalovirus (CMV), and Herpes Simplex Virus […]
Symptoms and Testing information for Tetanus Toxoid Antibody IgG Test
In the realm of preventive healthcare and diagnostics, the Tetanus Toxoid Antibody IgG Test emerges as a critical tool for assessing an individual’s immunity against tetanus, a potentially life-threatening condition caused by the bacterium Clostridium tetani. DNA Labs UAE, a leading genetic testing facility, offers this essential test, enabling individuals to understand their immune status […]
Symptoms and Testing information for Testosterone Total Ultrasensitive Test
DNA Labs UAE is at the forefront of medical diagnostics, offering a wide array of genetic testing services designed to provide detailed insights into your health and wellbeing. Among the numerous tests available, the Testosterone Total Ultrasensitive Test stands out for its precision and importance in evaluating testosterone levels, which play a crucial role in […]
Symptoms and Testing information for Steroid Panel 21-Hydroxylase Deficiency Test
DNA Labs UAE is at the forefront of genetic testing, offering a wide array of services designed to provide insights into your health and genetic makeup. Among the various tests offered, the Steroid Panel 21-Hydroxylase Deficiency Test is a crucial diagnostic tool for individuals suspected of having 21-Hydroxylase Deficiency, a genetic disorder that affects the […]
Symptoms and Testing information for Sjogren’s Syndrome Antibodies Test
Sjogren’s Syndrome is an autoimmune disorder characterized by its hallmark symptoms of dry eyes and dry mouth. However, the condition can affect other parts of the body, leading to a wide array of symptoms. Understanding these symptoms is crucial for individuals suspecting they may have Sjogren’s Syndrome. DNA Labs UAE offers a comprehensive Sjogren’s Syndrome […]
Symptoms and Testing information for SCA-7 Spinocerebellar Ataxia ATXN7 Gene Mutation Test
Spinocerebellar Ataxia Type 7 (SCA-7) is a progressive, neurodegenerative disorder characterized by a wide array of symptoms that result from a mutation in the ATXN7 gene. This mutation leads to an abnormal expansion of CAG repeats within the gene, which in turn affects the normal function of the cerebellum and other parts of the brain, […]