Epilepsy, Rolandic [epilepsie Rolandova]
- Terms
-
BECTS
benigní dětská epilepsie s centrotemporálními hroty
benigní epilepsie s rolandickými hroty
benigní rolandická epilepsie
rolandická epilepsie
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BCECTS
BECTS
Benign Childhood Epilepsy With Centro-Temporal Spikes
Benign Epilepsy Of Childhood With Centrotemporal Spikes
Benign Epilepsy With Centrotemporal Spikes
Benign Rolandic Epilepsy
Benign Rolandic Epilepsy of Childhood
Centralopathic Epilepsy
Centrotemporal Epilepsy
Epilepsy, Centrotemporal
Rolands Epilepsy
Sylvian Epilepsy
Temporal-Central Focal Epilepsy
An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and DYSARTHRIA. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41)
- DUI
- D019305 MeSH Browser
- CUI
- M0028742
- Previous indexing
- Epilepsy, Partial (1986-1996)
- History note
- 1997
- Public note
- 1997
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications 3
- CN
- congenital
- DI
- diagnosis 4
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 1
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 1
- GE
- genetics 1
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology 2
- PC
- prevention & control
- PX
- psychology 2
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery 2
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Disease MeSH Browser
Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, Autosomal Dominant Disease MeSH Browser
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Disease MeSH Browser