Neurology Diseases

The GRM7 gene, linked to several neurodevelopmental and psychiatric conditions, has garnered significant attention in the realm of genetic research. Among these conditions are Autism Spectrum Disorder (ASD), hyperactivity disorders, and bipolar disorder. These conditions share a complex interplay of genetic and environmental factors, making their diagnosis and treatment challenging. Recognizing the symptoms associated with […]

At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals understand their genetic makeup and identify potential health risks. One of the specific tests we offer is for the RNF170 gene, which is associated with Ataxia Sensory Type 1, an autosomal dominant genetic condition. This test is crucial for […]

Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, leading to muscle weakness, loss of motor function, and, eventually, severe disability. Among the genetic factors contributing to ALS, mutations in the VPS54 gene have been identified as one of the rare causes. Understanding the symptoms […]

Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. This debilitating condition leads to the deterioration and death of motor neurons, which are essential for controlling muscle movement. When these neurons die, the brain’s ability to initiate and control muscle movement is lost. With […]

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 […]