Epilepsies, Myoclonic [epilepsie myoklonické]
- Terms
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benigní dětská myoklonická epilepsie
benigní dětské myoklonické epilepsie
epilepsie myoklonická
idiopatická myoklonická epilepsie
idiopatické myoklonické epilepsie
infantilní myoklonická epilepsie
infantilní myoklonické epilepsie
maligní infantilní myoklonická epilepsie
myoklonická absenční epilepsie
myoklonická encefalopatie
myoklonická epilepsie časného dětského věku
myoklonické encefalopatie
myoklonické epilepsie časného dětského věku
myoklonické epilepsie s absencemi
myoklonicko-astatická epilepsie
symptomatická myoklonická epilepsie
symptomatické myoklonické epilepsie
syndrom Dravetové
těžká myoklonická dětská epilepsie
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Benign Infantile Myoclonic Epilepsy
Cryptogenic Myoclonic Epilepsy
Doose Syndrome
Dravet Syndrome
Early Childhood Epilepsy, Myoclonic
Early Childhood, Myoclonic Epilepsy
Encephalopathy, Myoclonic
Epilepsy, Early Childhood, Myoclonic
Epilepsy, Myoclonic, Early Childhood
Epilepsy, Myoclonic, Infantile
Epilepsy, Myoclonic, Infantile, Benign
Epilepsy, Myoclonic, Infantile, Severe
Epilepsy, Myoclonus
Idiopathic Myoclonic Epilepsy
Infantile Severe Myoclonic Epilepsy
Myoclonic Absence Epilepsy
Myoclonic Astatic Epilepsy
Myoclonic Encephalopathy
Myoclonic Epilepsy
Myoclonic Epilepsy, Benign Infantile
Myoclonic Epilepsy, Early Childhood
Myoclonic Epilepsy, Infantile
Myoclonic Epilepsy, Infantile, Benign
Myoclonic Epilepsy, Infantile, Severe
Myoclonic Epilepsy, Severe Infantile
Myoclonic Epilepsy, Severe, Of Infancy
Myoclonic Seizure Disorder
Severe Infantile Myoclonic Epilepsy
Severe Myoclonic Epilepsy Of Infancy
Severe Myoclonic Epilepsy, Infantile
Symptomatic Myoclonic Epilepsy
A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic.
- DUI
- D004831 MeSH Browser
- CUI
- M0328686
- Previous indexing
- Epilepsy (1966-1976); Myoclonus (1966-1976)
- History note
- 2000(1992) was EPILEPSY, MYOCLONUS 1977-1991
- Public note
- 2000; see EPILEPSY, MYOCLONIC 1992-1999; see EPILEPSY, MYOCLONUS 1977-1991
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced 3
- CL
- classification 1
- CO
- complications 1
- CN
- congenital 1
- DI
- diagnosis 18
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 13
- EC
- economics 1
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 3
- EH
- ethnology
- ET
- etiology 6
- GE
- genetics 10
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing 1
- PS
- parasitology
- PA
- pathology 2
- PP
- physiopathology 11
- PC
- prevention & control 1
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 5
- UR
- urine
- VE
- veterinary
- VI
- virology
Ataxia with Myoclonic Epilepsy and Presenile Dementia Disease MeSH Browser
Deafness, Congenital, and Familial Myoclonic Epilepsy Disease MeSH Browser
Epilepsy, Familial Adult Myoclonic, 3 Disease MeSH Browser
Epilepsy, Myoclonic, Benign Adult Familial, Type 1 Disease MeSH Browser
Epilepsy, Myoclonic, Benign Adult Familial, Type 2 Disease MeSH Browser
Familial encephalopathy with neuroserpin inclusion bodies Disease MeSH Browser
Feigenbaum Bergeron Richardson syndrome Disease MeSH Browser
Hydroxylysinuria Disease MeSH Browser
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders Disease MeSH Browser
Myoclonic Epilepsy, Hartung Type Disease MeSH Browser
Photoparoxysmal Response 3 Disease MeSH Browser
Spastic Paraplegia With Myoclonic Epilepsy Disease MeSH Browser