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. This condition leads to muscle weakness, disability, and eventually, death. ALS is characterized by its heterogeneity, with numerous genetic variations contributing to its onset and progression. Among these genetic factors, […]
Understanding the APOE Gene and Its Role in Alzheimer’s Disease Type 2 The APOE gene is one of the most extensively studied genes in connection to Alzheimer’s disease. This gene comes in several variants, with APOE ε2, ε3, and ε4 being the most common. The presence of the APOE ε4 allele is known to increase […]
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. Type 18 ALS, specifically linked to mutations in the PFN1 gene, is one of the genetic forms of this condition. Understanding the symptoms of PFN1 Gene Amyotrophic Lateral Sclerosis […]
Symptoms of PSEN1 Gene Alzheimer Disease Type 3 Genetic Test Alzheimer’s disease is a progressive neurological disorder that leads to memory loss and a decline in cognitive abilities. Among its various forms, Alzheimer disease type 3, linked to mutations in the PSEN1 gene, is one of the most severe. Understanding the symptoms associated with this […]
Understanding PSEN2 Gene Alzheimer Disease Type 4 Alzheimer’s disease, a progressive neurodegenerative disorder, has long been a subject of extensive research within the medical community. Among its various forms, Alzheimer Disease Type 4, linked to the PSEN2 gene, stands out due to its genetic underpinnings. This condition not only affects individuals in their later stages […]
Alzheimer’s disease is a progressive neurological disorder that leads to memory loss and cognitive decline. Among the genetic factors contributing to the risk of developing Alzheimer’s, the SORL1 gene has been identified as a significant player, particularly in cases of early onset autosomal dominant Alzheimer’s disease. Recognizing the symptoms and understanding the importance of genetic […]
Alzheimer’s disease is a progressive neurodegenerative disorder that affects memory, thinking, and behavior. The discovery of genetic links to Alzheimer’s has opened new avenues for understanding the disease, leading to the development of genetic tests that can indicate an individual’s risk. One such gene of interest is the RTN3 gene. DNA Labs UAE offers a […]
Symptoms of ST3GAL5 Gene Amish Infantile Epilepsy Syndrome Amish Infantile Epilepsy Syndrome, also known as ST3GAL5 deficiency, is a rare genetic disorder that predominantly affects the Amish community. This condition is characterized by a spectrum of neurological symptoms, primarily due to mutations in the ST3GAL5 gene. Understanding the symptoms associated with this syndrome is crucial […]
— TTR Gene Amyloidosis is a progressively debilitating condition that affects various organs and tissues in the body. This genetic disorder is caused by mutations in the transthyretin (TTR) gene, which leads to the abnormal accumulation of amyloid proteins in the body’s organs and tissues, impairing their normal function. Recognizing the symptoms early is crucial […]
GSN Gene Amyloidosis, also known as Finnish type amyloidosis, is a rare genetic condition that predominantly affects individuals of Finnish descent but can also occur in other populations. This condition is caused by mutations in the GSN gene, which plays a crucial role in the body’s ability to break down and recycle proteins. When mutations […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
