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. It leads to the loss of muscle control, making it difficult for those affected to speak, eat, move, and eventually breathe. Among the various genetic forms of this condition, […]

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 14, associated with mutations in the VCP gene, is a rare form of this condition. Understanding the symptoms and undergoing genetic testing can be crucial for individuals […]

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. Among the various types of ALS, type 12, linked to mutations in the OPTN gene, is of particular interest to researchers and clinicians alike. DNA Labs UAE is at […]

Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. Among the various genetic mutations linked to ALS, mutations in the FIG4 gene are known to cause a rare subtype of the disease, referred to as ALS type 11. […]

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. Among the various genetic forms of ALS, type 10, caused by mutations in the TARDBP gene, is particularly noteworthy. Understanding the symptoms of TARDBP gene-related ALS and the importance […]

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, leading to muscle weakness, disability, and eventually, death. One of the genetic causes of ALS is mutations in the SOD1 gene, which accounts for about 20% of familial ALS cases […]

In the realm of genetic testing and diagnostics, DNA Labs UAE stands at the forefront, offering a plethora of tests designed to unveil the genetic predispositions to various health conditions. Among these, the CHGB Gene Amyotrophic Lateral Sclerosis Risk Factor Genetic Test is a critical tool in understanding the genetic risk factors associated with Amyotrophic […]

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 […]

— 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 […]

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 […]