Neurology Diseases

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 […]

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 […]

In the quest to understand and manage genetic disorders, the importance of accurate diagnosis cannot be overstated. One such condition that has garnered attention is the genetic disorder associated with the COX20 gene, which can lead to symptoms such as ataxia and muscle hypotonia. DNA Labs UAE is at the forefront of providing comprehensive genetic […]

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Among its various types, ALS type 8, caused by mutations in the VAPB gene, presents unique challenges and symptoms for those affected. DNA Labs UAE offers a comprehensive genetic test for this specific type of […]

At DNA Labs UAE, we are committed to providing advanced genetic testing services to help identify various genetic disorders, including the ANG Gene Amyotrophic Lateral Sclerosis Type 9 (ALS9). This particular genetic test is crucial for individuals who have a family history of ALS or exhibit symptoms associated with this condition. ALS, also known as […]

Amyotrophic lateral sclerosis (ALS), often referred to 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 atrophy. When ALS is found alongside frontotemporal dementia (FTD), a condition characterized by changes in personality, behavior, and language due to the degeneration of […]

Symptoms of SS18L1 Gene Amyotrophic Lateral Sclerosis CREST Related Genetic Test 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. A variant of ALS has been linked to mutations in the SS18L1 gene, and understanding the symptoms related […]