Ataxia-Telangiectasia (A-T) is a rare, genetic disorder that affects various parts of the body and leads to severe disability. A-T is characterized by progressive cerebellar ataxia, telangiectasia, immune defects, and a predisposition to malignancy. Advances in genetic testing, particularly Next Generation Sequencing (Nx Gen Sequencing), have made it possible to diagnose this condition with greater […]
Neurology Diseases
Symptoms and Testing information for Nx Gen Sequencing Charcot-Marie-Tooth Disease and Sensory Neuropathies Test
Charcot-Marie-Tooth disease (CMT) is a group of inherited disorders that affect the peripheral nerves, which are located outside the brain and spinal cord. These disorders are characterized by a progressive loss of muscle tissue and touch sensation across various parts of the body. Sensory neuropathies, on the other hand, primarily affect the sensory nerves, leading […]
Symptoms and Testing information for Nx Gen Sequencing Comprehensive Epilepsy Test
In the realm of medical diagnostics, the advancement of genetic testing has been a beacon of hope for countless individuals and families affected by genetic disorders. Among these advancements, Next Generation Sequencing (NGS) stands out, especially in the field of neurology, where it has revolutionized the diagnosis and understanding of epilepsy. DNA Labs UAE, a […]
Symptoms and Testing information for Nx Gen Sequencing Dementia Test
Dementia is a collective term used to describe various symptoms of cognitive decline, such as forgetfulness. It is a symptom of several underlying diseases and brain disorders. Understanding and diagnosing dementia early can significantly affect the management and progression of the condition. DNA Labs UAE is at the forefront of providing advanced diagnostic solutions, including […]
Symptoms and Testing information for Nx Gen Sequencing Dravet’s Syndrome and Early Infantile Epileptic Encephalopathy Test
Symptoms of Nx Gen Sequencing Dravet’s Syndrome and Early Infantile Epileptic Encephalopathy Dravet’s Syndrome and Early Infantile Epileptic Encephalopathy (EIEE) are two severe neurological conditions that manifest in early childhood. Both conditions are characterized by frequent seizures, developmental delays, and cognitive impairments. Understanding the symptoms of these disorders is crucial for early diagnosis and management. […]
Symptoms and Testing information for POLG Gene Alper’s Syndrome Genetic Test
Understanding the genetic underpinnings of various diseases has become a cornerstone of modern medicine, enabling more precise diagnoses, personalized treatments, and better patient outcomes. Among the numerous conditions being explored through genetic testing, POLG gene-related Alper’s Syndrome stands out due to its complexity and the critical need for early diagnosis. At DNA Labs UAE, we […]
Symptoms and Testing information for Meningoencephalitis Advantage Test
Meningoencephalitis is a serious condition that combines the characteristics of both meningitis and encephalitis, where the brain and the membranes that surround it become inflamed. This inflammation can be caused by infections, autoimmune diseases, or other conditions. Recognizing the symptoms early can lead to prompt treatment, which is crucial for a positive outcome. DNA Labs […]
Symptoms and Testing information for Meningoencephalitis Panel CSF Test
In the realm of medical diagnostics, the precision and speed at which conditions can be identified are paramount. Among the numerous tests that have become essential in the quick diagnosis and treatment of severe conditions is the Meningoencephalitis Panel CSF Test. This test is a critical tool in the arsenal of healthcare professionals for the […]
Symptoms and Testing information for Nx Gen Sequencing Familial Hemiplegic Migraine Test
Familial Hemiplegic Migraine (FHM) is a rare form of migraine headache that is accompanied by hemiparesis (weakness on one side of the body) during the aura phase of the migraine. This condition is primarily genetic, and advancements in genetic testing have made it possible to identify the mutations associated with FHM. DNA Labs UAE is […]
Symptoms and Testing information for PEX26 Gene Zellweger Syndrome Genetic Test
Understanding the symptoms of PEX26 Gene Zellweger Syndrome is crucial for early diagnosis and management of the condition. Zellweger Syndrome, a rare genetic disorder, affects multiple systems in the body and is characterized by the absence of functional peroxisomes in the cells. The PEX26 gene plays a significant role in the biogenesis of peroxisomes, and […]