Search on: BENIGN CHILDHOOD EPILEPSY WITH CENTRO-TEMPORAL SPIKES 
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Descriptor English:   Epilepsy, Rolandic 
Descriptor Spanish:   Epilepsia Rolándica 
Descriptor Portuguese:   Epilepsia Rolândica 
Synonyms English:   Rolands Epilepsy
Benign Childhood Epilepsy With Centro-Temporal Spikes
Benign Rolandic Epilepsy of Childhood
Epilepsy, Centrotemporal
Sylvian Epilepsy  
Tree Number:   C10.228.140.490.360.280
Definition English:   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. The episodes tend to occur at night and may become secondarily generalized. In most cases, affected children are neurologically and developmentally normal. The electroencephalogram shows characteristic high-voltage sharp waves over the central temporal regions, which are more prominent during drowsiness and sleep. In general, seizures do not continue beyond mid-adolescence. (From Epilepsia 1998 39;Suppl 4:S32-S41) 
History Note English:   1997 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
congenital complications
diet therapy diagnosis
drug therapy economics
ethnology embryology
enzymology epidemiology
etiology genetics
history immunology
metabolism microbiology
mortality nursing
pathology prevention & control
physiopathology parasitology
psychology radiography
rehabilitation radionuclide imaging
radiotherapy surgery
therapy urine
ultrasonography veterinary
virology  
Record Number:   32946 
Unique Identifier:   D019305 

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