Early infantile epileptic encephalopathy (EIEE), also known as Ohtahara Syndrome, is a rare and severe form of epilepsy that appears in the first few months of life, often leading to serious developmental delays and neurological issues. One of the genetic causes linked to this condition is mutations in the AARS1 gene, which is critical for […]
Understanding the complexities of genetic conditions is crucial in providing timely and effective care for affected individuals. One such condition that has garnered attention within the medical community is Early Infantile Epileptic Encephalopathy Type 3 (EIEE3), which is associated with mutations in the SLC25A22 gene. DNA Labs UAE offers a comprehensive genetic test for this […]
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 […]
Understanding the symptoms and early diagnosis of genetic disorders is crucial in providing effective treatment and improving the quality of life for those affected. Among the various genetic conditions, Early Infantile Epileptic Encephalopathy Type 19 (EIEE19), associated with mutations in the GABRA1 gene, is particularly challenging due to its early onset and severe symptoms. DNA […]
Understanding the symptoms and the importance of early detection in conditions like Early Infantile Epileptic Encephalopathy Type 2 (EIEE2), also known as CDKL5 deficiency disorder, is crucial for parents and caregivers. This rare genetic disorder is characterized by early onset, difficult-to-control seizures, and severe neurodevelopmental impairment. Recognizing the symptoms early on can lead to a […]
Understanding the TAF1 Gene DYT3 Genetic Test At DNA Labs UAE, we are committed to providing advanced genetic testing services to help individuals understand their genetic makeup and manage potential health risks effectively. One such genetic test we offer is the TAF1 Gene DYT3 Genetic Test, which is crucial for diagnosing a rare neurological disorder […]
Understanding the genetic underpinnings of various medical conditions is crucial for early diagnosis and effective treatment. One such condition, Early Infantile Epileptic Encephalopathy Type 20 (EIEE20), is linked to mutations in the PIGA gene. DNA Labs UAE is at the forefront of genetic testing for this condition, providing hope and answers to affected families. This […]
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.
