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 […]
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 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, […]
Spinocerebellar ataxia type 6 (SCA-6) is a progressive neurodegenerative disorder that is part of a larger group of genetic conditions known as the spinocerebellar ataxias. This particular type is caused by a specific mutation in the CACNA1A gene, which plays a crucial role in the normal functioning of nerve cells in the brain. Understanding the […]
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 […]
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 […]
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 […]
In the realm of genetic diagnostics, understanding and identifying the symptoms of various genetic disorders is crucial for early intervention and management. One such disorder, Spinocerebellar Ataxia Type 1 (SCA-1), stems from mutations in the ATXN1 gene. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including the SCA-1 Spinocerebellar Ataxia […]
In the realm of prenatal diagnostics and maternal health, the Placental Growth Factor (PlGF) test has emerged as a pivotal tool for assessing the risk of certain conditions during pregnancy, such as preeclampsia. DNA Labs UAE, a premier genetic laboratory, offers this advanced testing option to support expectant mothers and healthcare providers in managing pregnancy […]
Symptoms of Mycobacterium Tuberculosis rRNA Detection TMA Test Mycobacterium tuberculosis is the bacterium responsible for tuberculosis (TB), a disease that primarily affects the lungs but can also impact other parts of the body. Identifying the presence of this bacterium early is crucial for effective treatment and control of the disease. The Mycobacterium Tuberculosis rRNA Detection […]
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.
