Global genomic collaboration provides diagnos
A technique known as rapid genome sequencing has provided a diagnosis for 43 per cent of infants with unexplained epilepsy and informed their care in an international partnership.
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A technique known as rapid genome sequencing has provided a diagnosis for 43 per cent of infants with unexplained epilepsy and informed their care in an international partnership.
Epilepsy in infants ranges in severity and can leave caregivers with questions about their child's health. While genetic testing to help determine the cause of epilepsy is possible, comprehensive testing does not always happen routinely and it can take a long time, leaving families waiting for answers.
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Paul's Purple Warriors and Epilepsy Services of New Jersey held the third annual Seize the Wave event Tuesday on the 37th Street beach. The event allows children with epilepsy to
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