The SCN2A gene is critical in the development and function of the nervous system, playing a pivotal role in the regulation of electrical signals in the brain. Mutations in this gene are linked to a range of neurological conditions, including Convulsions Benign Familial Infantile 3 (BFIC3). This condition, while rare, is significant for the families […]
Neurology Diseases
Symptoms and Testing information for EGR2 Gene Dejerine-Sottas Disease Genetic Test
Symptoms of EGR2 Gene Dejerine-Sottas Disease Genetic Test Dejerine-Sottas Disease (DSD), also known as Hereditary Motor and Sensory Neuropathy Type III, is a rare genetic disorder that affects the peripheral nervous system. It is caused by mutations in several genes, including the EGR2 gene. This condition is characterized by a progressive loss of muscle tissue […]
Symptoms and Testing information for PRRT2 Gene Convulsions Familial Infantile with Paroxysmal Choreoathetosis Genetic Test
Understanding PRRT2 Gene Convulsions: Familial Infantile with Paroxysmal Choreoathetosis Convulsions and movement disorders in infants can be alarming for parents and caregivers, signaling the need for immediate medical attention and accurate diagnosis. One such condition that has gained attention in the medical community is related to the PRRT2 gene, known for causing Familial Infantile Convulsions […]
Symptoms and Testing information for GJB1 Gene Dejerine-Sottas Disease Genetic Test
Dejerine-Sottas Disease, also known as hereditary motor and sensory neuropathy type III, is a progressive neurological disorder that affects the peripheral nerves. It is characterized by severe muscle weakness and sensory loss in the limbs. The GJB1 gene plays a crucial role in the development of this condition, and genetic testing can provide valuable insights […]
Symptoms and Testing information for IGBP1 Gene Corpus Callosum Agenesis of with Mental Retardation Ocular Coloboma and Micrognathia Genetic Test
Understanding the IGBP1 Gene and Its Implications The human genome is a complex blueprint of life, containing the instructions needed for the development, functioning, and reproduction of humans. Within this vast network of genetic information, certain genes play critical roles in the development of the brain and other organs. One such gene is the IGBP1 […]
Symptoms and Testing information for MPZ Gene Dejerine-Sottas Disease Genetic Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive range of services designed to provide individuals with crucial insights into their genetic makeup. Among the various tests offered, the MPZ Gene Dejerine-Sottas Disease Genetic Test is a critical tool for diagnosing Dejerine-Sottas Disease (DSD), a rare genetic disorder that […]
Symptoms and Testing information for TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Genetic Test
Certainly! Here is the article in the requested format: Understanding TUBB3 Gene Cortical Dysplasia Complex with Other Brain Malformations Type 1 Cortical dysplasia complex with other brain malformations type 1, associated with mutations in the TUBB3 gene, represents a significant concern in neurodevelopmental disorders. This condition, often abbreviated as CDCBM1, is characterized by a range […]
Symptoms and Testing information for PMP22 Gene Dejerine-Sottas Disease Genetic Test
Symptoms of PMP22 Gene Dejerine-Sottas Disease Genetic Test Dejerine-Sottas Disease, also known as hereditary motor and sensory neuropathy type III, is a rare genetic disorder that affects the peripheral nervous system. It is caused by mutations in the PMP22 gene, among others, and leads to severe neurological problems. Understanding the symptoms of this condition is […]
Symptoms and Testing information for TUBB2A Gene Cortical Dysplasia Complex with Other Brain Malformations Type 5 Genetic Test
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help diagnose and understand a variety of genetic conditions. One of the specialized tests we offer focuses on the TUBB2A gene, which is associated with Cortical Dysplasia Complex with Other Brain Malformations Type 5. This condition is a rare but serious […]
Symptoms and Testing information for CNTNAP2 Gene Cortical Dysplasia-Focal Epilepsy Syndrome Genetic Test
Understanding the complexities of genetic conditions is crucial for early diagnosis and effective management. One such complex condition is Cortical Dysplasia-Focal Epilepsy Syndrome, which is associated with mutations in the CNTNAP2 gene. At DNA Labs UAE, we provide a comprehensive genetic test for this syndrome, aiming to offer insights and guidance for affected individuals and […]