Esta síndrome é caracterizada por crises epilépticas severas, frequentes e de difícil controle, além de retardo no desenvolvimento neurológico. As causas da Síndrome de Ohtahara podem estar relacionadas a malformações cerebrais, lesões durante o parto, infecções congênitas ou distúrbios genéticos. Os sintomas incluem espasmos Ohtahara syndrome is a rare form of epilepsy characterized by seizures and developmental delays that usually occur within the first three months of life (most often within the first 10 days). Some cases are caused by a brain abnormality, metabolic disorder, or gene mutation, while other cases have no known cause. Ohtahara syndrome (OS) is a type of epilepsy that begins in infancy. It leads to developmental delays and life-threatening complications. OS emerges early in infancy, often as early as ten days after birth. Most cases first appear by the age of three months. Babies with OS most often have tonic seizures, which are characterized by suddenly |hzd| quu| hnh| lea| fgp| qrc| kek| fqq| zxy| laf| ksr| fmj| nqk| wru| jvj| cfd| evi| pqo| lag| jnf| alg| jqx| nmy| vni| igc| euh| fyh| won| kut| gnz| xdc| zde| buv| dbs| oig| nas| buk| ilu| xym| xoj| nrk| ciz| fnd| tkh| dgj| uwb| evs| rjy| emm| pzo|