Neurology Diseases

Understanding the genetic underpinnings of autism spectrum disorder (ASD) has been a focal point of contemporary medical research. Among the numerous genes associated with ASD, the CHD8 gene has garnered significant attention. Mutations in the CHD8 gene have been linked to a specific subtype of autism known as CHD8 Autism Susceptibility Type 18. DNA Labs […]

Symptoms of GYG2 Gene Autism 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 role of genetics in autism is significant, with numerous genes implicated in its development. One such gene is GYG2, which has recently been linked to […]

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 […]

Symptoms of PIK3R5 Gene Ataxia-Oculomotor Apraxia Type 3 Genetic Test Ataxia-Oculomotor Apraxia Type 3 (AOA3) is a rare genetic disorder that affects the nervous system, leading to a variety of symptoms that can significantly impact an individual’s quality of life. This condition is caused by mutations in the PIK3R5 gene, which plays a crucial role […]

At DNA Labs UAE, we are dedicated to providing advanced genetic testing services to help individuals and families understand their genetic makeup and its implications on their health. One of the specialized tests we offer is the PNKP Gene Ataxia-Oculomotor Apraxia Type 4 Genetic Test. This test is crucial for diagnosing Ataxia-Oculomotor Apraxia Type 4 […]

Ataxia-Telangiectasia (A-T) is a rare, neurodegenerative, inherited disease that affects several organs in the body. It is primarily characterized by progressive cerebellar ataxia, telangiectasias, immune defects, and a predisposition to malignancy. This condition is caused by mutations in the ATM gene, which plays a critical role in cell cycle control, DNA repair, and cellular response […]

Attention Deficit-Hyperactivity Disorder (ADHD) is a neurodevelopmental disorder characterized by an ongoing pattern of inattention and/or hyperactivity-impulsivity that interferes with functioning or development. While ADHD is often thought of as a childhood disorder, it can continue into adulthood and throughout a person’s life. In recent years, there has been a growing interest in the genetic […]

Attention Deficit-Hyperactivity Disorder (ADHD) is a neurodevelopmental disorder characterized by a pattern of behavior that can include difficulty in maintaining attention, hyperactivity, and impulsiveness that is more pronounced than typically observed in individuals at a comparable level of development. While the exact cause of ADHD is not fully understood, research has identified a strong genetic […]

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 symptoms are usually seen in the early developmental period. However, they may not fully manifest until social demands exceed limited capacities. Recent advancements in genetics have led to the identification of […]

Autism Spectrum Disorder (ASD) is a complex neurodevelopmental disorder characterized by a wide range of symptoms and levels of impairment. Genetic factors play a significant role in the development of ASD, and recent advances in genetic testing have made it possible to identify specific genetic markers associated with the disorder. One such marker is the […]