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 […]











