Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations

By |2017-02-17T18:00:21-05:00February 17th, 2017|Categories: DSF Research Review|Tags: , , |

(Cetica, 2017). Now that genetic testing is becoming more common and less expensive, more infants under 12 months are being tested for SCN1A mutations. For infants who are positive for SCN1A mutations, the question of how those mutations will present clinically remains to be answered at such a young age. In this study of medical [...]