Which condition is known for frequent sever seizures and cognitive decline in children?

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Rasmussen's encephalitis is characterized by frequent severe seizures and notable cognitive decline in children. This neurological condition is marked by unilateral inflammation of the brain, which leads to the degeneration of brain tissue in one hemisphere. The seizures associated with this condition are often refractory, meaning that they do not respond well to conventional anti-seizure medications, and the frequency and severity of these seizures can significantly impact cognitive development and overall functioning.

The cognitive decline seen in Rasmussen's encephalitis is largely due to the progressive atrophy of affected brain tissue, which impairs motor, cognitive, and sensory functions. Over time, children with this condition may exhibit significant developmental delays or a decline in previously acquired skills, necessitating a multidisciplinary approach to care, including medical management and potential surgical interventions like hemispherectomy in extreme cases.

Other conditions listed have different characteristics. For example, Reye's syndrome primarily involves liver dysfunction and acute encephalopathy due to metabolic issues, Todd's paralysis is a temporary neurological deficit following seizures, and Sturge-Weber syndrome features a facial birthmark and neurological symptoms associated with vascular malformations. Each of these conditions has distinct clinical presentations that do not specifically encompass severe, frequent seizures coupled with cognitive decline in the same manner as Rasmussen's encephal

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