Neurology Diseases

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 […]

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 […]

Symptoms of PRPS1 Gene Arts Syndrome Genetic Test Arts Syndrome is a rare genetic disorder caused by mutations in the PRPS1 gene. This condition is characterized by a range of symptoms that affect multiple systems within the body. Recognizing the symptoms early on can lead to a timely diagnosis, which is crucial for managing the […]

Amyotrophic lateral sclerosis (ALS) type 4, caused by mutations in the SETX gene, is a rare and hereditary form of ALS that is characterized by its adult-onset and progressive nature. Understanding the symptoms and opting for genetic testing can play a crucial role in managing this condition. DNA Labs UAE offers a comprehensive SETX Gene […]

Asperger syndrome, now considered part of the broader category of Autism Spectrum Disorder (ASD), is a complex and multifaceted condition that affects individuals differently. The identification of genetic markers associated with Asperger syndrome has been a significant step forward in understanding its complexities. Among these genetic markers, the NLGN3 gene plays a crucial role. DNA […]

Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive neurodegenerative disorder that affects nerve cells in the brain and the spinal cord. ALS type 6, associated with mutations in the FUS gene, is one of the genetic forms of this condition. Recognizing the symptoms of this specific type of ALS is […]