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. […]
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Symptoms and Testing information for SLC25A22 Gene Early infantile epileptic encephalopathy type 3 Genetic Test
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 and Testing information for AARS1 Gene Early infantile epileptic encephalopathy type 29 Genetic Test
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 […]
Symptoms and Testing information for WWOX Gene Early infantile epileptic encephalopathy type 28 Genetic Test
Understanding the genetic underpinnings of neurological disorders has become a pivotal aspect of modern medicine, offering insights into diagnosis, management, and potential treatment options. Among these, the WWOX gene’s role in early infantile epileptic encephalopathy type 28 (EIEE28) has garnered significant attention. This condition, characterized by severe neurological impairment beginning in infancy, necessitates a comprehensive […]
Symptoms and Testing information for GRIN2B Gene Early infantile epileptic encephalopathy type 27 Genetic Test
— Understanding the symptoms of GRIN2B Gene Early Infantile Epileptic Encephalopathy Type 27 is crucial for early diagnosis and management. This condition, also known as EIEE27, is a severe neurological disorder that affects infants shortly after birth. DNA Labs UAE offers a comprehensive genetic test for this condition, providing essential information for affected families. EIEE27 […]
Symptoms and Testing information for KCNB1 Gene Early infantile epileptic encephalopathy type 26 Genetic Test
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 factors contributing to this condition, mutations in the KCNB1 gene have been identified as a cause of EIEE type 26. Understanding the symptoms and undergoing […]
Symptoms and Testing information for SLC13A5 Gene Early infantile epileptic encephalopathy type 25 Genetic Test
Understanding the symptoms and the importance of early detection for SLC13A5 Gene Early Infantile Epileptic Encephalopathy Type 25 is crucial for parents and healthcare providers. This condition, more commonly referred to as EIEE25, is a rare genetic disorder that affects the nervous system, leading to severe epilepsy and developmental delays from infancy. DNA Labs UAE […]
Symptoms and Testing information for HCN1 Gene Early infantile epileptic encephalopathy type 24 Genetic Test
Early Infantile Epileptic Encephalopathy (EIEE) represents a group of severe brain disorders that manifest in the first few months of life, often characterized by frequent seizures and significant developmental delays. One specific form of this condition, known as Early Infantile Epileptic Encephalopathy Type 24 (EIEE24), is linked to mutations in the HCN1 gene. Understanding the […]
Symptoms and Testing information for DOCK7 Gene Early infantile epileptic encephalopathy type 23 Genetic Test
Understanding the symptoms of specific genetic conditions is crucial for early diagnosis and management. One such condition is Early Infantile Epileptic Encephalopathy Type 23 (EIEE23), which is associated with mutations in the DOCK7 gene. This condition, characterized by early-onset seizures and developmental delay, poses significant challenges to affected individuals and their families. Recognizing the symptoms […]
Symptoms and Testing information for NECAP1 Gene Early infantile epileptic encephalopathy type 21 Genetic Test
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 […]