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, […]
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 […]
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 […]
In the realm of genetic testing and diagnosis, advancements have paved the way for identifying and understanding a myriad of genetic disorders that were once shrouded in mystery. Among these, Spinocerebellar Ataxia Type 2 (SCA-2) stands out as a condition that can significantly impact an individual’s quality of life. This neurological disorder, linked to the […]
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 […]
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. […]
Understanding SCA-12 Spinocerebellar Ataxia Spinocerebellar Ataxia Type 12 (SCA-12) is a progressive neurodegenerative disorder characterized by a wide range of symptoms that primarily affect an individual’s motor skills. It is caused by a mutation in the PPP2R2B gene located on chromosome 5. This condition is part of a group of genetic disorders known as spinocerebellar […]
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 […]
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 […]
Spinocerebellar Ataxia Type 3 (SCA-3), also known as Machado-Joseph Disease, is a rare, inherited neurodegenerative disorder that affects the cerebellum—the part of the brain that controls muscle movement. It is caused by a mutation in the ATXN3 gene, which leads to the abnormal function of ataxin-3 protein, thereby affecting the nervous system and leading to […]
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.
