Neurology Diseases

Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) is a genetic disorder that affects the peripheral nerves, which are responsible for sending signals between the brain and the muscles, as well as sensory information back to the brain. This condition is caused by mutations in the PMP22 gene, which plays a crucial role in the […]

Understanding the complexities of genetic conditions is crucial for early diagnosis and treatment. One such condition that has garnered attention in the medical community is POLG gene neuropathy with sensory ataxic dysarthria and ophthalmoparesis. This genetic disorder, although rare, presents a spectrum of symptoms that can significantly impact an individual’s quality of life. In response […]

Understanding the intricate nature of genetic conditions is pivotal in the realm of medical science. Among these conditions, neurodevelopmental disorders and microcephaly present significant challenges to affected individuals and their families. The KIF5C gene plays a crucial role in the normal development of the brain, and mutations in this gene can lead to severe neurodevelopmental […]

Understanding the symptoms of GTPBP2 gene neurodegeneration with brain iron accumulation and the significance of GTPBP2 related genetic testing is crucial for early diagnosis and management of this condition. DNA Labs UAE offers a comprehensive genetic test for this purpose, priced at 4400 AED. This article delves into the symptoms associated with the disorder, the […]

Symptoms of TUBG1 Gene Neurodevelopmental Malformation and Microcephaly Genetic Test Understanding the symptoms and genetic underpinnings of neurodevelopmental disorders is crucial for early diagnosis and intervention. One such condition, characterized by neurodevelopmental malformations and microcephaly, is linked to mutations in the TUBG1 gene. DNA Labs UAE offers a comprehensive genetic test to identify mutations in […]

Understanding BRAT1 Gene Neurodevelopmental Disorder The BRAT1 gene neurodevelopmental disorder, also known as rigidity and multifocal seizure syndrome, neonatal onset, or early infantile epileptic encephalopathy 61, is a rare but severe condition that significantly impacts the central nervous system. This disorder is characterized by a range of symptoms, including cerebellar atrophy, which can lead to […]

DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide individuals with the most accurate and detailed genetic information. One of the specialized tests offered by DNA Labs UAE is the DES Gene Neurogenic Scapuloperoneal Syndrome Kaeser Type Genetic Test. This test is crucial for individuals […]

The ADAM22 gene plays a critical role in the development and function of the nervous system. Mutations or alterations in this gene can lead to a range of neurodevelopmental disorders, which may affect an individual’s cognitive, social, and motor skills. Recognizing the symptoms associated with ADAM22 gene neurodevelopmental disorder is crucial for early diagnosis and […]

Neuromyotonia and axonal neuropathy, also known as HINT1 neuropathy, is a rare genetic condition that affects the peripheral nervous system. This disorder is characterized by a range of symptoms that can significantly impact the quality of life of those affected. It is caused by mutations in the HINT1 gene and is inherited in an autosomal […]

Understanding the complex world of genetics can be daunting, yet it is crucial for the diagnosis and management of various genetic disorders. Among these, neurodevelopmental disorders represent a significant category that affects countless families worldwide. The APC2 gene has been identified as a key player in one such disorder, shedding light on the importance of […]