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 […]
Neuronal migration disorders are a group of conditions caused by the abnormal migration of neurons in the developing brain and nervous system. Among these disorders, mutations in the CTNNA2 gene have been identified as a significant contributor. The CTNNA2 gene plays a critical role in the development and function of the nervous system. Its mutations […]
Symptoms of CNTNAP4 Gene Neurodevelopmental Disorder The CNTNAP4 gene plays a critical role in the development of the nervous system and its proper functioning. Mutations in this gene can lead to a variety of neurodevelopmental disorders, which can affect an individual’s life in numerous ways. Understanding the symptoms associated with these disorders is crucial for […]
Understanding the symptoms of CROCC gene neurodevelopmental disorder is crucial for early diagnosis and intervention. This genetic condition, linked to the CROCC gene, affects neurological development and can have a range of impacts on an individual’s cognitive, motor, and social abilities. DNA Labs UAE offers a comprehensive genetic test specifically designed to identify mutations in […]
Neurodevelopmental disorders are a group of conditions that affect the development of the nervous system, leading to abnormal brain function which can manifest as psychiatric issues, learning difficulties, and impairments in motor function. Among the various genetic factors contributing to these disorders, mutations in the FRMPD4 gene have been identified as a significant cause. Understanding […]
Symptoms of KCTD3 Gene Neurodevelopmental Disorder The KCTD3 gene is known to play a critical role in the normal development of the nervous system. Mutations in the KCTD3 gene can lead to a rare but significant neurodevelopmental disorder, which manifests through a variety of symptoms. Recognizing these symptoms early can be crucial for timely intervention […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
