Early Infantile Epileptic Encephalopathy (EIEE), also known as Ohtahara Syndrome, is a severe neurological disorder that appears in the early stages of infancy, often within the first few months of life. Among the genes associated with this condition, the SIK1 gene has been identified as a significant contributor to the development of EIEE type 30. […]
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 various genetic factors that contribute to this condition, mutations in the DNM1 gene have been identified as a cause of EIEE type 31. Understanding the symptoms […]
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 […]
Understanding the complexities of our genetic makeup has become a pivotal aspect of modern healthcare, offering insights into a variety of genetic conditions that affect individuals in different ways. One such condition that has garnered attention in the realm of genetic research is related to mutations in the TUBB4A gene, known to be associated with […]
Early infantile epileptic encephalopathy (EIEE), also known as Ohtahara Syndrome, is a rare neurological disorder characterized by severe seizures and significant developmental delays. Type 21 of this condition, specifically linked to mutations in the NECAP1 gene, presents unique challenges and symptoms for affected infants. Recognizing these symptoms early on is crucial for managing the condition […]
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.
