The SLC2A1 gene plays a critical role in the human body, particularly in the transport of glucose across the blood-brain barrier. Mutations in this gene can lead to a variety of neurological conditions, one of which is DYT8, also known as Paroxysmal Exercise-Induced Dyskinesia (PED). Understanding the symptoms associated with SLC2A1 gene mutations is crucial […]
Understanding the nuances and implications of genetic conditions is crucial for early diagnosis and treatment. Among these conditions, Early Infantile Epileptic Encephalopathy Type 1 (EIEE1), associated with mutations in the ARX gene, stands out due to its severe impact on affected infants. DNA Labs UAE offers comprehensive genetic testing for this condition, providing essential information […]
Understanding the symptoms and early diagnosis of genetic conditions is paramount in providing the necessary interventions and care. One such condition is Early Infantile Epileptic Encephalopathy Type 10 (EIEE10), associated with mutations in the PNKP gene. DNA Labs UAE is at the forefront of offering comprehensive genetic testing services, including the PNKP Gene Early Infantile […]
Understanding the intricacies of genetic disorders is crucial for early diagnosis and effective management. One such complex condition is Early Infantile Epileptic Encephalopathy Type 11 (EIEE11), associated with mutations in the SCN2A gene. This condition is a severe form of epilepsy that manifests in the early stages of infancy and is characterized by frequent seizures […]
Understanding the PLCB1 Gene and Its Impact on Early Infantile Epileptic Encephalopathy Type 12 Early infantile epileptic encephalopathy (EIEE), also known as Ohtahara Syndrome, represents one of the most severe forms of epilepsy syndromes that appear in infancy. Among the genes implicated in this condition, the PLCB1 gene plays a crucial role. Mutations in the […]
Understanding the complexities of genetic conditions is pivotal for early diagnosis and management. Among these conditions, Early Infantile Epileptic Encephalopathy Type 13 (EIEE13), caused by mutations in the SCN8A gene, is a severe disorder that demands attention. This condition is characterized by frequent seizures that begin in the first days or months of life, developmental […]
Symptoms of KCNT1 Gene Early Infantile Epileptic Encephalopathy Type 14 Early Infantile Epileptic Encephalopathy (EIEE), also known as Ohtahara Syndrome, is a severe form of epilepsy that appears in the first few months of a child’s life. Among the genetic causes identified for this condition, mutations in the KCNT1 gene have been associated with EIEE […]
Understanding the symptoms of Early Infantile Epileptic Encephalopathy Type 15 (EIEE15) is crucial for early diagnosis and management. This rare but severe condition is caused by mutations in the ST3GAL3 gene, which plays a significant role in brain development. DNA Labs UAE offers a comprehensive genetic test for identifying mutations in the ST3GAL3 gene, aiding […]
Early Infantile Epileptic Encephalopathy (EIEE), also known as Ohtahara Syndrome, is a severe form of epilepsy that appears in the first few months of a child’s life. Among the genes linked to this condition, TBC1D24 plays a significant role. Mutations in the TBC1D24 gene can lead to Early Infantile Epileptic Encephalopathy Type 16 (EIEE16), a […]
Understanding the complexities of genetic disorders is crucial for early diagnosis and management. Among these, the GNAO1 gene mutation leading to Early Infantile Epileptic Encephalopathy Type 17 (EIEE17) is a significant concern for many parents and healthcare providers. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including tests for the […]
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.
