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 […]
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 […]
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 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 […]
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 […]
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 […]
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 […]
Neurodegeneration with brain iron accumulation (NBIA) represents a group of rare, genetic neurological disorders characterized by abnormal accumulation of iron in the basal ganglia, a part of the brain that controls movement, resulting in progressive dystonia, spasticity, parkinsonism, neuropsychiatric abnormalities, and optic atrophy. One specific form of this disorder, known as COASY Protein-Associated Neurodegeneration (CoPAN), […]
Symptoms of C19orf12 Gene Neurodegeneration with Brain Iron Accumulation Type 4 Genetic Test Neurodegeneration with brain iron accumulation (NBIA) represents a group of rare, genetic neurological disorders characterized by abnormal accumulation of iron in the basal ganglia, a part of the brain that controls movement, leading to progressive dystonia, spasticity, and parkinsonism. Among the different […]
Neurodegeneration with Brain Iron Accumulation (NBIA) represents a group of rare, genetic neurological disorders characterized by abnormal accumulation of iron in the basal ganglia, a part of the brain that controls movement, leading to progressive dystonia, spasticity, parkinsonism, neuropsychiatric abnormalities, and optic atrophy. Type 5 NBIA, caused by mutations in the WDR45 gene, is particularly […]
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.
