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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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Study investigates the impact of rapid genome sequencing for infantile epilepsy

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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Global genomic collaboration provides diagnos

Global genomic collaboration provides diagnos
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Global Genomic Alliance Aids Infant Epilepsy Diagnosis, Care

Global Genomic Alliance Aids Infant Epilepsy Diagnosis, Care
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