Search on: BENIGN EPILEPSY WITH CENTROTEMPORAL SPIKES 
Descriptors Found: 1
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Descriptor English:   Epilepsy, Rolandic 
Descriptor Spanish:   Epilepsia Rolándica 
Descriptor Portuguese:   Epilepsia Rolândica 
Synonyms English:   BCECTS
BECTS
Benign Epilepsy Of Childhood With Centrotemporal Spikes
Benign Rolandic Epilepsy
Centralopathic Epilepsy
Centrotemporal Epilepsy
Temporal-Central Focal Epilepsy
Benign Childhood Epilepsy With Centro Temporal Spikes
Centralopathic Epilepsies
Centrotemporal Epilepsies
Epilepsies, Centralopathic
Epilepsies, Centrotemporal
Epilepsies, Rolandic
Epilepsy, Benign Rolandic
Epilepsy, Centralopathic
Epilepsy, Rolands
Epilepsy, Sylvian
Rolandic Epilepsies
Rolandic Epilepsy
Rolandic Epilepsy, Benign
Rolands Epilepsy
Benign Childhood Epilepsy With Centro-Temporal Spikes
Benign Epilepsy With Centrotemporal 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. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41) 
History Note English:   1997 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DG diagnostic imaging
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RT radiotherapy RH rehabilitation
SU surgery TH therapy
UR urine VE veterinary
VI virology  
Record Number:   32946 
Unique Identifier:   D019305 

Occurrence in VHL: 		 

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