DNA Labs UAE is at the forefront of genetic testing and diagnostics, providing a comprehensive range of services designed to offer insights into various genetic conditions. Among these, the APTX Gene Ataxia-Oculomotor Apraxia Type 1 Genetic Test is a critical tool for individuals suspecting they might be affected by this rare but impactful genetic disorder. […]
At DNA Labs UAE, we understand the importance of accurate and reliable genetic testing for conditions like Ataxia-Oculomotor Apraxia Type 2 (AOA2), caused by mutations in the SETX gene. This rare condition is part of a group of disorders that affect the nervous system, leading to a progressive loss of muscle control and coordination. Recognizing […]
Amyotrophic lateral sclerosis-parkinsonism/dementia complex (ALS-PDC) is a rare neurodegenerative disorder that poses significant challenges to individuals affected by it. This condition, characterized by a combination of amyotrophic lateral sclerosis (ALS), parkinsonism, and dementia, has been linked to genetic factors, including mutations in the TRPM7 gene. Understanding the symptoms associated with this condition and the importance […]
In the realm of genetic research and testing, the advancement in identifying specific genes responsible for hereditary conditions has been groundbreaking. One such significant discovery is the identification of the 9-Sep gene, which is linked to Amyotrophy Hereditary Neuralgic, a rare but severe neurological disorder. DNA Labs UAE is at the forefront of providing comprehensive […]
Angelman syndrome is a complex genetic disorder that primarily affects the nervous system. Characterized by a range of physical and neurological problems, this condition is often associated with delays in development, issues with speech and balance, intellectual disability, and sometimes, seizures. Recognizing the symptoms early can be crucial for managing the condition effectively. DNA Labs […]
Angelman syndrome is a complex genetic disorder that primarily affects the nervous system. Characterized by severe developmental delays, problems with speech and balance, intellectual disability, and sometimes, seizures, it is a condition that has profound implications for affected individuals and their families. One of the critical steps in diagnosing this syndrome is identifying mutations or […]
Symptoms of CDKL5 Gene Angelman-like syndrome Genetic Test The CDKL5 Gene Angelman-like Syndrome is a rare genetic disorder that affects the development of the nervous system, leading to a range of neurological and developmental challenges. This condition, often characterized by early-onset seizures, severe intellectual disability, and motor impairment, demands accurate diagnosis for effective management and […]
Amyotrophic Lateral Sclerosis Type 2 (ALS2), also known as juvenile ALS, is a rare and severe neurological disorder that primarily affects the nerve cells responsible for controlling voluntary muscle movement. This condition is characterized by the gradual degeneration and death of motor neurons, leading to muscle weakness and atrophy. ALS2 is caused by mutations in […]
Understanding the complexities of genetic conditions is pivotal in providing the right care and interventions for those affected. One such condition that has garnered attention in the medical community is MECP2 gene-related Angelman-like syndrome. This rare genetic disorder shares similarities with Angelman syndrome, primarily affecting neurological development. Recognizing the symptoms and undergoing timely genetic testing […]
Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive neurodegenerative disorder that affects nerve cells in the brain and spinal cord, leading to muscle weakness and, eventually, loss of muscle control. One of the genetic variants associated with this condition is linked to the MATR3 gene, which can lead to a […]
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.
