Genetic mutations associated with epileptic encephalopathies presenting in infancy | ||||||
---|---|---|---|---|---|---|
Mutation Site | Ohtahara Syndrome | EME | West Syndrome | SMEI | Atypical RTT with Early Epilepsy | EFMR |
ARX | Yes | Yes | ||||
CDKL5 | Yes | Yes | ||||
ErbB4 | Yes | |||||
MAGI2 | Yes | |||||
PCDH19 | Yes | Yes | ||||
PNKP | Yes | Yes | ||||
SCN1A | Yes | |||||
SLC25 A22 | Yes | |||||
STXBP1 | Yes | Yes |
Source[1]