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Rapid DNA sequencing yields timely answers for infant epilepsy

A pilot cohort study on infants with new-onset epilepsy examines the clinical utility of rapid genome sequencing

The clinical impact of rapid genome sequencing of infants with new-onset epilepsy.

Rapid Genome Sequencing Expedites Epilepsy, Seizure Diagnosis in Infants

Using rapid genome sequencing, researchers evaluate the impact of an expedited genetic diagnosis of infantile epilepsy.

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.

Global genomic collaboration provides diagnoses and informs care for infants with epilepsy