— Alzheimer’s disease is a progressive neurological disorder that leads to memory loss and cognitive decline. Among the genetic factors contributing to the disease, mutations in the APP gene are significant for early-onset Alzheimer’s disease type 1. DNA Labs UAE offers a comprehensive genetic test for individuals who want to assess their risk for this […]
Neurology Diseases
Symptoms and Testing information for VCP Gene Amyotrophic lateral sclerosis type 14 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. 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 […]
Symptoms and Testing information for ABCD1 Gene AdrenoleukodystrophyAdrenomyeloneuropathy Genetic Test
Adrenoleukodystrophy (ALD) and adrenomyeloneuropathy (AMN) are genetically inherited conditions that affect the nervous system and adrenal glands, stemming from mutations in the ABCD1 gene. These conditions can lead to a wide range of symptoms, affecting both physical and neurological functions. Understanding these symptoms is crucial for early detection and management of the conditions. DNA Labs […]
Symptoms and Testing information for SLC12A6 Gene Agenesis of the corpus callosum with peripheral neuropathy Genetic Test
Understanding the complexities of genetic conditions is crucial for early diagnosis and treatment. Among these, the agenesis of the corpus callosum with peripheral neuropathy, related to mutations in the SLC12A6 gene, stands out due to its unique combination of neurological symptoms. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including […]
Symptoms and Testing information for TREX1 Gene Aicardi-Goutieres syndrome type 1 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, immune system, and skin. It is a condition that typically presents in infancy or early childhood and can result in a range of neurological and physical symptoms. One of the genes associated with this condition is the TREX1 gene, and mutations in this […]
Symptoms and Testing information for RNASEH2B Gene Aicardi-Goutieres syndrome type 2 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, the immune system, and the skin. Among the various genes associated with this condition, mutations in the RNASEH2B gene lead to what is specifically known as AGS type 2. This particular type of AGS manifests through a range of symptoms that can significantly […]
Symptoms and Testing information for RNASEH2C Gene Aicardi-Goutieres syndrome type 3 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, immune system, and skin. Among the different types of AGS, Type 3 is particularly associated with mutations in the RNASEH2C gene. This condition is known for its early onset, often presenting symptoms in infancy or early childhood, which can significantly impact the quality […]
Symptoms and Testing information for RNASEH2A Gene Aicardi-Goutieres syndrome type 4 Genetic Test
In the intricate world of genetic disorders, Aicardi-Goutieres syndrome (AGS) stands out due to its complexity and the range of symptoms it presents. AGS is a rare, genetically inherited disease that mimics congenital viral infections without an actual infection, leading to significant neurological and immune system dysfunction. Among the genes associated with AGS, mutations in […]
Symptoms and Testing information for SAMHD1 Gene Aicardi-Goutieres syndrome type 5 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, immune system, and skin. Among the different types of AGS, Type 5 is particularly associated with mutations in the SAMHD1 gene. This condition is characterized by a range of symptoms that can significantly impact the quality of life of affected individuals and their […]
Symptoms and Testing information for ADAR Gene Aicardi-Goutieres syndrome type 6 Genetic Test
Aicardi-Goutieres Syndrome (AGS) is a rare genetic disorder that affects the brain, the immune system, and the skin. Type 6 of this syndrome, specifically, is caused by mutations in the ADAR gene. This condition is characterized by a variety of symptoms that can significantly impact the quality of life for those affected. Recognizing these symptoms […]