“Missing Mutation” Found in Severe Infant Epilepsy
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CHOP has found a long-suspected “missing mutation” in severe infant epilepsy, with early hints that anti-seizure drugs might help patients.
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CHOP has found a long-suspected “missing mutation” in severe infant epilepsy, with early hints that anti-seizure drugs might help patients.
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Before starting on the ketogenic diet, Tikvah suffered from intractable absence seizures. But after just two months on the diet, her condition dramatically improved.
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The Pediatric Epilepsy Program is one of the largest and most interdisciplinary programs of its kind in the world, with expertise covering all aspects of epilepsy management.
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Experts from Children’s Hospital of Philadelphia’s Pediatric Epilepsy Program present on a variety of topics at the American Epilepsy Society Annual Meeting.
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Novel technologies have helped researchers identify more than 30 new genes that cause epilepsy and led neurologists at CHOP to pioneer new diagnostic technologies and treatments.
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The Children’s Hospital of Philadelphia is one of only a handful of pediatric hospitals in the country to offer transcranial magnetic stimulation (TMS) to localize the epileptogenic and sensorimotor cortical regions in order to improve family counseling regarding epilepsy surgery and help surgeons avoid those areas when operating.
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Neurologists at CHOP published a case study of a young patient with MPSI found to have an activating mutation in KCNT1 who showed a dramatic reduction in seizure frequency and improvement in psychomotor and language skills after treatment with quinidine.
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The Children's Hospital of Philadelphia will be a site for a Phase III clinical trial to test the efficacy of a cannabis extract for treating severe childhood epilepsy.
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An attending physician in The Children’s Hospital of Philadelphia’s Division of Neurology dedicates his current research to investigating how epilepsy works, in hopes of discovering an altogether new way to treat the condition.