Neurology Diseases

— Symptoms of ASPA Gene Canavan Disease Genetic Test Canavan Disease is a rare inherited disorder that affects the brain and the central nervous system’s ability to send and receive messages. It is caused by mutations in the ASPA gene, which leads to a deficiency of the enzyme aspartoacylase. This deficiency results in the accumulation […]

In the realm of genetic testing and diagnostics, understanding the intricate connections between genes and various health conditions has become paramount. Among the various genes under scrutiny for their role in developmental and neurological disorders, the RNF128 gene has garnered significant attention, particularly in its association with autism spectrum disorders (ASD). DNA Labs UAE, a […]

Autism Spectrum Disorder (ASD) is a complex developmental condition that involves persistent challenges in social interaction, speech and nonverbal communication, and restricted/repetitive behaviors. The ways in which ASD manifests can vary greatly among individuals and across the lifespan. Recent advancements in genetics have begun to uncover the genetic underpinnings of autism, leading to more personalized […]

Symptoms of SETD2 Gene Autism Autism Spectrum Disorder (ASD) is a complex developmental condition that involves persistent challenges in social interaction, speech and nonverbal communication, and restricted/repetitive behaviors. The effects of ASD and the severity of symptoms are different in each person. One of the genetic markers associated with autism is the SETD2 gene. The […]

Autism Spectrum Disorder (ASD) is a complex developmental condition that involves persistent challenges in social interaction, speech, and nonverbal communication, along with restricted/repetitive behaviors. The symptoms are usually seen in the early developmental period. However, the intensity and manifestation of these symptoms can vary widely among individuals. Recent advancements in genetic research have led to […]

In the realm of genetic testing and diagnostics, the identification of specific genes related to autism spectrum disorder (ASD) represents a significant advancement. One such gene, UNC13B, has been associated with an increased risk of developing ASD. At DNA Labs UAE, we are at the forefront of providing comprehensive genetic testing services, including the UNC13B […]

In the quest to understand the complex world of autism spectrum disorder (ASD), scientists and researchers have been diligently exploring the genetic underpinnings that might contribute to its development. One such genetic marker that has come under scrutiny is the ZNF778 gene. DNA Labs UAE, a leading genetic laboratory, offers a comprehensive ZNF778 Related Genetic […]

Understanding the complex nature of genetic disorders is a challenging yet crucial aspect of modern medicine. Among these, the ATP10A gene’s role in autism, mental retardation, and susceptibility to Angelman Syndrome has garnered significant attention. DNA Labs UAE, a pioneering genetic testing facility, offers a comprehensive test designed to identify mutations in the ATP10A gene. […]

Symptoms of COL6A1 Gene Bethlem Myopathy Genetic Test Bethlem myopathy, a disorder affecting the connective tissue, primarily muscles, is linked to mutations in the COL6A1 gene. Recognizing the symptoms early can significantly impact management and quality of life. DNA Labs UAE offers a genetic test for the COL6A1 gene mutation, pivotal in diagnosing Bethlem myopathy. […]

Bethlem myopathy, a rare genetic disorder, falls under the umbrella of collagen VI-related myopathies. This condition is primarily characterized by muscle weakness and joint stiffness (contractures), typically manifesting from early childhood, although symptoms can appear at any age. The COL6A2 gene plays a critical role in the development and functioning of muscles and connective tissues […]