Vertaling van "epilepsy with myoclonic absences " (Engels → Frans) :

TERMINOLOGIE

Epilepsy with:myoclonic absences | myoclonic-astatic seizures | Infantile spasms Lennox-Gastaut syndrome Salaam attacks Symptomatic early myoclonic encephalopathy West's syndrome
Encéphalopathie myoclonique précoce symptomatique Epilepsie avec:absences myocloniques | crises astato-myocloniques | Spasmes infantiles Syndrome de:Lennox-Gastaut | West | Tic de Salaam

myoclonic absence | complex absence with myoclonus | myoclonic petit mal
absence myoclonique | absence clonique

Benign:myoclonic epilepsy in infancy | neonatal convulsions (familial) | Childhood absence epilepsy [pyknolepsy] Epilepsy with grand mal seizures on awakening Juvenile:absence epilepsy | myoclonic epilepsy [impulsive petit mal] | Nonspecific epileptic seizures:atonic | clonic | myoclonic | tonic | tonic-clonic
Convulsions néonatales bénignes (familiales) Crises non spécifiques:atoniques | cloniques | myocloniques | tonico-cloniques | toniques | Epilepsie (avec):absences de l'adolescence | absences de l'enfance [pyknolepsie] | crises [grand mal] au réveil | myoclonique bénigne de l'enfance | myoclonique [petit mal impulsif] juvénile

impulsive petit-mal | Janz syndrome | juvenile myoclonic epilepsy
épilepsie impulsive

intermittent myoclonic epilepsy
épilepsie intermittente myoclonique de Rabot

myoclonic epilepsy
épilepsie myoclonique

A rare epilepsy syndrome with characteristics of recurrent, long-lasting myoclonic status in infants and young children with a non-progressive encephalopathy, associated with transient and recurring motor, cognitive and/or behavioral disturbances.
epilepsie myoclonique des encéphalopathies non-progressives

A rare epilepsy syndrome characterised by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behaviour problems are frequentl
spasme infantile à début tardif

A rare epilepsy syndrome characterized by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently
spasme cryptogénique à début tardif

IN-CONTEXT TRANSLATIONS

1 || KIEKIDS || 2011 || To develop an innovative, age-adapted, flexible and safe paediatric formulation of ethosuximide for the treatment of absence and of myoclonic epilepsies in children || NA
1 || KIEKIDS || 2011 || Développer une formulation pédiatrique innovante, adaptée à l’âge, flexible et sûre de l’éthosuximide pour le traitement de l’absence épileptique et de l’épilepsie myoclonique chez les enfants || N/A