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A new drug, zorevunersen, reduces seizures by up to 90% in children with Dravet syndrome, offering hope for a transformative treatment.
A new drug, zorevunersen, is showing significant promise in treating Dravet syndrome, a severe genetic epilepsy affecting children.
Administered via spinal injection, it boosts healthy sodium channels in the brain, reducing seizures by up to 90% in early trials.
Children as young as two in the UK and US have experienced dramatic improvements, including fewer seizures and better quality of life.
Phase Three trials are underway to confirm long-term safety and effectiveness, with experts calling the results a transformative breakthrough for families affected by the condition.
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Un nuevo fármaco, zorevunersen, reduce las convulsiones hasta en un 90% en niños con síndrome de Dravet, ofreciendo esperanzas de un tratamiento transformador.