Search on: ROLANDS EPILEPSY 
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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 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 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 RA radiography
RI radionuclide imaging RT radiotherapy
RH rehabilitation SU surgery
TH therapy US ultrasonography
UR urine VE veterinary
VI virology  
Record Number:   32946 
Unique Identifier:   D019305 

Occurrence in VHL:
 

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