Epilepsy, Rolandic [epilepsie Rolandova]

topical
7
Terms

BECTS
benigní dětská epilepsie s centrotemporálními hroty
benigní epilepsie s rolandickými hroty
benigní rolandická epilepsie
rolandická epilepsie

 

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

Persistent link   https://www.medvik.cz/link/D019305
Definition

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

C Diseases
C10.228.140 Brain Diseases 1 183
C10.228.140.490 Epilepsy 3 266
C10.228.140.490.360 Epilepsies, Partial 193
C10.228.140.490.360.260 Epilepsy, Complex Partial 15
C10.228.140.490.360.270 Epilepsy, Frontal Lobe 11
C10.228.140.490.360.272 Epilepsy, Partial, Motor 9
C10.228.140.490.360.275 Epilepsy, Partial, Sensory 6
C10.228.140.490.360.280 Epilepsy, Rolandic 7
C10.228.140.490.360.290 Epilepsy, Temporal Lobe 194
C10.228.140.490.493 Epileptic Syndromes 21
C10.228.140.490.493.063 Epilepsies, Myoclonic 46
C10.228.140.490.493.125 Epilepsy, Absence 47
C10.228.140.490.493.188 Epilepsy, Frontal Lobe 11
C10.228.140.490.493.250 Epilepsy, Rolandic 7
C10.228.140.490.493.375 Epilepsy, Temporal Lobe 194
C10.228.140.490.493.500 Landau-Kleffner Syndrome 16
C10.228.140.490.493.750 Lennox Gastaut Syndrome 6
C10.228.140.490.493.875 Spasms, Infantile 112

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