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Benign myoclonic epilepsy in infancy
Childhood absence epilepsy
Clonic
Early myoclonic encephalopathy
Epilepsy with myoclonic absences
Impulsive petit mal
Myoclonic
Myoclonic epilepsy
Myoclonic epilepsy in non-progressive encephalopathy
Myoclonic-astatic seizures
Neonatal convulsions
Nonspecific epileptic seizures atonic
Progressive myoclonic epilepsy
Pyknolepsy
Tonic
Tonic-clonic

Translation of "myoclonic epilepsy " (English → French) :

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
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
WORLD HEALTH ORGANIZATION ICD-10: G40.3
WORLD HEALTH ORGANIZATION ICD-10: G40.3
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Myoclonic epilepsy in non-progressive encephalopathy
https://browser.ihtsdotools.or (...) (...) [HTML]
epilepsie myoclonique des encéphalopathies non-progressives
SNOMEDCT-BE (disorder) / 778047006
SNOMEDCT-BE (disorder) / 778047006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce
SNOMEDCT-BE (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome / 771469002
SNOMEDCT-BE (disorder) / 771469002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Progressive myoclonic epilepsy
https://browser.ihtsdotools.or (...) (...) [HTML]
épilepsie myoclonique progressive
SNOMEDCT-BE (disorder) / 267581004
SNOMEDCT-BE (disorder) / 267581004
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Epilepsy with:myoclonic absences | myoclonic-astatic seizures | Infantile spasms Lennox-Gastaut syndrome Salaam attacks Symptomatic early myoclonic encephalopathy West's syndrome
https://icd.who.int/browse10/2 (...) (...) [HTML]
Encéphalopathie myoclonique précoce symptomatique Epilepsie avec:absences myocloniques | crises astato-myocloniques | Spasmes infantiles Syndrome de:Lennox-Gastaut | West | Tic de Salaam
WORLD HEALTH ORGANIZATION ICD-10: G40.4
WORLD HEALTH ORGANIZATION ICD-10: G40.4
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
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.
https://browser.ihtsdotools.or (...) (...) [HTML]
epilepsie myoclonique des encéphalopathies non-progressives
SNOMEDCT-CA (trouble) / 778047006
SNOMEDCT-CA (trouble) / 778047006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Benign childhood epilepsy with centrotemporal EEG spikes Childhood epilepsy with occipital EEG paroxysms
https://icd.who.int/browse10/2 (...) (...) [HTML]
Epilepsie bénigne de l'enfant avec pointes-ondes centro-temporales à l'EEG [Loiseau-Beaussart] Epilepsie de l'enfant avec paroxysmes occipitaux à l'EEG
WORLD HEALTH ORGANIZATION ICD-10: G40.0
WORLD HEALTH ORGANIZATION ICD-10: G40.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
A cerebral malformation with epilepsy with predominant characteristics of posterior isolated lissencephaly with developmental delay, intellectual disability and epilepsy that usually evolves from West syndrome to Lennox-Gastaut syndrome. Additional f
https://browser.ihtsdotools.or (...) (...) [HTML]
lissencéphalie par mutation de LIS1
SNOMEDCT-BE (disorder) / 770560008
SNOMEDCT-BE (disorder) / 770560008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Early myoclonic encephalopathy
https://browser.ihtsdotools.or (...) (...) [HTML]
encéphalopathie myoclonique précoce
SNOMEDCT-BE (disorder) / 44423001
SNOMEDCT-BE (disorder) / 44423001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A rare chromosomal anomaly syndrome resulting from a partial interstitial deletion of the short arm of chromosome 9. The disease has characteristics of mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivi
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome de microdélétion 9p13
SNOMEDCT-BE (disorder) / 764725008
SNOMEDCT-BE (disorder) / 764725008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : benign myoclonic epilepsy in infancy    childhood absence epilepsy    early myoclonic encephalopathy    epilepsy with myoclonic absences    myoclonic epilepsy in non-progressive encephalopathy    nonspecific epileptic seizures atonic    progressive myoclonic epilepsy    clonic    impulsive petit mal    myoclonic    myoclonic epilepsy    myoclonic-astatic seizures    neonatal convulsions    pyknolepsy    tonic-clonic    


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'myoclonic epilepsy'

Date index:2022-06-17 -

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